Variant: rs1554109707 

    present in Gene: FLT4
    present in Chromosome: 5
    Position on Chromosome: 180613051
    Alleles of this Variant: C/G;T

rs1554109707 in FLT4 gene and Dysmorphic features PMID 19002718 2009 Analysis of the coding regions of VEGFR3 and VEGFC in Milroy disease and other primary lymphoedemas.

PMID 24167460 2013 Mutations in the VEGFR3 signaling pathway explain 36% of familial lymphedema.

PMID 23074044 2013 FLT4/VEGFR3 and Milroy disease: novel mutations, a review of published variants and database update.

PMID 9817924 1998 Hereditary lymphedema: evidence for linkage and genetic heterogeneity.

PMID 15689446 2005 Milroy disease and the VEGFR-3 mutation phenotype.

PMID 12960217 2003 Identification of eight novel VEGFR-3 mutations in families with primary congenital lymphoedema.

rs1554109707 in FLT4 gene and Multiple congenital anomalies PMID 9817924 1998 Hereditary lymphedema: evidence for linkage and genetic heterogeneity.

PMID 12960217 2003 Identification of eight novel VEGFR-3 mutations in families with primary congenital lymphoedema.

PMID 24167460 2013 Mutations in the VEGFR3 signaling pathway explain 36% of familial lymphedema.

PMID 15689446 2005 Milroy disease and the VEGFR-3 mutation phenotype.

PMID 19002718 2009 Analysis of the coding regions of VEGFR3 and VEGFC in Milroy disease and other primary lymphoedemas.

PMID 23074044 2013 FLT4/VEGFR3 and Milroy disease: novel mutations, a review of published variants and database update.

rs1554109707 in FLT4 gene and Muscle hypotonia PMID 15689446 2005 Milroy disease and the VEGFR-3 mutation phenotype.

PMID 9817924 1998 Hereditary lymphedema: evidence for linkage and genetic heterogeneity.

PMID 19002718 2009 Analysis of the coding regions of VEGFR3 and VEGFC in Milroy disease and other primary lymphoedemas.

PMID 24167460 2013 Mutations in the VEGFR3 signaling pathway explain 36% of familial lymphedema.

PMID 23074044 2013 FLT4/VEGFR3 and Milroy disease: novel mutations, a review of published variants and database update.

PMID 12960217 2003 Identification of eight novel VEGFR-3 mutations in families with primary congenital lymphoedema.