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rs587777711

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587777711(-;-)
Make rs587777711(-;G)
ReferenceGRCh38 38.1/142
Chromosome18
Position22172216
GeneGATA6
is asnp
is mentioned by
dbSNPrs587777711
ebirs587777711
HLIrs587777711
Exacrs587777711
Varsomers587777711
Maprs587777711
PheGenIrs587777711
hapmaprs587777711
1000 genomesrs587777711
hgdprs587777711
ensemblrs587777711
gopubmedrs587777711
geneviewrs587777711
scholarrs587777711
googlers587777711
pharmgkbrs587777711
gwascentralrs587777711
openSNPrs587777711
23andMers587777711
23andMe allrs587777711
SNP Nexus

SNPshotrs587777711
SNPdbers587777711
MSV3drs587777711
GWAS Ctlgrs587777711
Max Magnitude0
ClinVar
Risk rs587777711(;)
Alt rs587777711(;)
Reference rs587777711(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.19752177delG
CLNSRC OMIM Allelic Variant
CLNACC RCV000144068.2, RCV000191917.1,