Condition: Goldenhar Syndrome
rs3754648
in
AGAP1
gene and
Goldenhar Syndrome
PMID 26853712
2016 Genome-wide association study identifies multiple susceptibility loci for craniofacial microsomia.
rs10459648
in
ARID3B
gene and
Goldenhar Syndrome
PMID 26853712
2016 Genome-wide association study identifies multiple susceptibility loci for craniofacial microsomia.
rs4750407
in
FRMD4A
gene and
Goldenhar Syndrome
PMID 26853712
2016 Genome-wide association study identifies multiple susceptibility loci for craniofacial microsomia.
rs17802111
in
LOC101926974
gene and
Goldenhar Syndrome
PMID 26853712
2016 Genome-wide association study identifies multiple susceptibility loci for craniofacial microsomia.
rs17090300
in
LOC107984024;LINC00393;LINC00392
gene and
Goldenhar Syndrome
PMID 26853712
2016 Genome-wide association study identifies multiple susceptibility loci for craniofacial microsomia.
rs754423
in
NID2
gene and
Goldenhar Syndrome
PMID 26853712
2016 Genome-wide association study identifies multiple susceptibility loci for craniofacial microsomia.
rs7420812
in
PARD3B
gene and
Goldenhar Syndrome
PMID 26853712
2016 Genome-wide association study identifies multiple susceptibility loci for craniofacial microsomia.
rs3923380
in
SHROOM3
gene and
Goldenhar Syndrome
PMID 26853712
2016 Genome-wide association study identifies multiple susceptibility loci for craniofacial microsomia.