Condition: Gastroesophageal reflux disease
rs7609078
in
AFF3
gene and
Gastroesophageal reflux disease
PMID 31527586
2019 Gastroesophageal reflux GWAS identifies risk loci that also associate with subsequent severe esophageal diseases.
rs11901649
in
APOB
gene and
Gastroesophageal reflux disease
PMID 31527586
2019 Gastroesophageal reflux GWAS identifies risk loci that also associate with subsequent severe esophageal diseases.
rs597808
in
ATXN2
gene and
Gastroesophageal reflux disease
PMID 31527586
2019 Gastroesophageal reflux GWAS identifies risk loci that also associate with subsequent severe esophageal diseases.
rs7282609
in
C21orf62-AS1;LOC105377136
gene and
Gastroesophageal reflux disease
PMID 31527586
2019 Gastroesophageal reflux GWAS identifies risk loci that also associate with subsequent severe esophageal diseases.
rs7552188
in
DPYD
gene and
Gastroesophageal reflux disease
PMID 31527586
2019 Gastroesophageal reflux GWAS identifies risk loci that also associate with subsequent severe esophageal diseases.
rs10228350
in
FOXP2
gene and
Gastroesophageal reflux disease
PMID 31527586
2019 Gastroesophageal reflux GWAS identifies risk loci that also associate with subsequent severe esophageal diseases.
rs12706746
in
GRM8
gene and
Gastroesophageal reflux disease
PMID 31527586
2019 Gastroesophageal reflux GWAS identifies risk loci that also associate with subsequent severe esophageal diseases.
rs9266237
in
HLA-B
gene and
Gastroesophageal reflux disease
PMID 31527586
2019 Gastroesophageal reflux GWAS identifies risk loci that also associate with subsequent severe esophageal diseases.
rs12974777
in
KLHL26
gene and
Gastroesophageal reflux disease
PMID 31527586
2019 Gastroesophageal reflux GWAS identifies risk loci that also associate with subsequent severe esophageal diseases.
rs10940767
in
LINC02109
gene and
Gastroesophageal reflux disease
PMID 31527586
2019 Gastroesophageal reflux GWAS identifies risk loci that also associate with subsequent severe esophageal diseases.
rs4721096
in
LOC100127955;MAD1L1
gene and
Gastroesophageal reflux disease
PMID 31527586
2019 Gastroesophageal reflux GWAS identifies risk loci that also associate with subsequent severe esophageal diseases.
rs34796998
in
LOC105371829
gene and
Gastroesophageal reflux disease
PMID 31527586
2019 Gastroesophageal reflux GWAS identifies risk loci that also associate with subsequent severe esophageal diseases.
rs4362541
in
LOC105374786;LINC02831
gene and
Gastroesophageal reflux disease
PMID 31527586
2019 Gastroesophageal reflux GWAS identifies risk loci that also associate with subsequent severe esophageal diseases.
rs2971030
in
LOC105375146
gene and
Gastroesophageal reflux disease
PMID 29551738
2018 Interactions Between Genetic Variants and Environmental Factors Affect Risk of Esophageal Adenocarcinoma and Barrett's Esophagus.
rs7763910
in
LOC285819;BTN2A1
gene and
Gastroesophageal reflux disease
PMID 31527586
2019 Gastroesophageal reflux GWAS identifies risk loci that also associate with subsequent severe esophageal diseases.
rs809955
in
MAML3
gene and
Gastroesophageal reflux disease
PMID 31527586
2019 Gastroesophageal reflux GWAS identifies risk loci that also associate with subsequent severe esophageal diseases.
rs7141987
in
MIR329-2;MIR323A;MIR329-1;MIR758;MEG8;MIR1197
gene and
Gastroesophageal reflux disease
PMID 29551738
2018 Interactions Between Genetic Variants and Environmental Factors Affect Risk of Esophageal Adenocarcinoma and Barrett's Esophagus.
rs1937450
in
PDE4B
gene and
Gastroesophageal reflux disease
PMID 31527586
2019 Gastroesophageal reflux GWAS identifies risk loci that also associate with subsequent severe esophageal diseases.
rs397507545
in
PTPN11
gene and
Gastroesophageal reflux disease
PMID 12717436
2003 Somatic mutations in PTPN11 in juvenile myelomonocytic leukemia, myelodysplastic syndromes and acute myeloid leukemia.
PMID 15928039
2005 The mutational spectrum of PTPN11 in juvenile myelomonocytic leukemia and Noonan syndrome/myeloproliferative disease.
PMID 15001945
2004 Genotype-phenotype correlations in Noonan syndrome.
PMID 16358218
2006 Diversity and functional consequences of germline and somatic PTPN11 mutations in human disease.
rs11171710
in
RAB5B
gene and
Gastroesophageal reflux disease
PMID 31527586
2019 Gastroesophageal reflux GWAS identifies risk loci that also associate with subsequent severe esophageal diseases.
rs80338796
in
RAF1
gene and
Gastroesophageal reflux disease
PMID 17603483
2007 Gain-of-function RAF1 mutations cause Noonan and LEOPARD syndromes with hypertrophic cardiomyopathy.
PMID 17603482
2007 Germline gain-of-function mutations in RAF1 cause Noonan syndrome.
rs10242223
in
SDK1
gene and
Gastroesophageal reflux disease
PMID 31527586
2019 Gastroesophageal reflux GWAS identifies risk loci that also associate with subsequent severe esophageal diseases.
rs74652506
in
SNRK;ANO10
gene and
Gastroesophageal reflux disease
PMID 31527586
2019 Gastroesophageal reflux GWAS identifies risk loci that also associate with subsequent severe esophageal diseases.