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rs387906814

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs387906814(C;G)
Make rs387906814(G;G)
ReferenceGRCh38 38.1/141
Chromosome18
Position22171736
GeneGATA6
is asnp
is mentioned by
dbSNPrs387906814
ebirs387906814
HLIrs387906814
Exacrs387906814
Varsomers387906814
Maprs387906814
PheGenIrs387906814
hapmaprs387906814
1000 genomesrs387906814
hgdprs387906814
ensemblrs387906814
gopubmedrs387906814
geneviewrs387906814
scholarrs387906814
googlers387906814
pharmgkbrs387906814
gwascentralrs387906814
openSNPrs387906814
23andMers387906814
23andMe allrs387906814
SNP Nexus

SNPshotrs387906814
SNPdbers387906814
MSV3drs387906814
GWAS Ctlgrs387906814
Max Magnitude0
ClinVar
Risk rs387906814(G;G)
Alt rs387906814(G;G)
Reference rs387906814(C;C)
Significance Pathogenic
Disease Tetralogy of Fallot
Variation info
Gene GATA6
CLNDBN Tetralogy of Fallot
Reversed 0
HGVS NC_000018.9:g.19751697C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000023129.3,