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rs797045792

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs797045792(G;T)
Make rs797045792(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position173232990
GeneNKX2-5
is asnp
is mentioned by
dbSNPrs797045792
ebirs797045792
HLIrs797045792
Exacrs797045792
Varsomers797045792
Maprs797045792
PheGenIrs797045792
hapmaprs797045792
1000 genomesrs797045792
hgdprs797045792
ensemblrs797045792
gopubmedrs797045792
geneviewrs797045792
scholarrs797045792
googlers797045792
pharmgkbrs797045792
gwascentralrs797045792
openSNPrs797045792
23andMers797045792
23andMe allrs797045792
SNP Nexus

SNPshotrs797045792
SNPdbers797045792
MSV3drs797045792
GWAS Ctlgrs797045792
Max Magnitude0
ClinVar
Risk rs797045792(T;T)
Alt rs797045792(T;T)
Reference rs797045792(G;G)
Significance Pathogenic
Disease Malformation of the heart and great vessels
Variation info
Gene NKX2-5
CLNDBN Malformation of the heart and great vessels
Reversed 1
HGVS NC_000005.9:g.172659993C>A
CLNSRC
CLNACC RCV000193839.1,