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rs587777710

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587777710(G;T)
Make rs587777710(T;T)
ReferenceGRCh38 38.1/142
Chromosome18
Position22171856
GeneGATA6
is asnp
is mentioned by
dbSNPrs587777710
ebirs587777710
HLIrs587777710
Exacrs587777710
Varsomers587777710
Maprs587777710
PheGenIrs587777710
hapmaprs587777710
1000 genomesrs587777710
hgdprs587777710
ensemblrs587777710
gopubmedrs587777710
geneviewrs587777710
scholarrs587777710
googlers587777710
pharmgkbrs587777710
gwascentralrs587777710
openSNPrs587777710
23andMers587777710
23andMe allrs587777710
SNP Nexus

SNPshotrs587777710
SNPdbers587777710
MSV3drs587777710
GWAS Ctlgrs587777710
Max Magnitude0
ClinVar
Risk rs587777710(T;T)
Alt rs587777710(T;T)
Reference rs587777710(G;G)
Significance Pathogenic
Disease Pancreatic agenesis and congenital heart disease Congenital diaphragmatic hernia Malformation of the heart and great vessels
Variation info
Gene GATA6
CLNDBN Pancreatic agenesis and congenital heart disease Congenital diaphragmatic hernia Malformation of the heart and great vessels
Reversed 0
HGVS NC_000018.9:g.19751817G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000144067.2, RCV000191916.1,