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rs797045791

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs797045791(G;G)
Make rs797045791(G;T)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position173233032
GeneNKX2-5
is asnp
is mentioned by
dbSNPrs797045791
ebirs797045791
HLIrs797045791
Exacrs797045791
Varsomers797045791
Maprs797045791
PheGenIrs797045791
hapmaprs797045791
1000 genomesrs797045791
hgdprs797045791
ensemblrs797045791
gopubmedrs797045791
geneviewrs797045791
scholarrs797045791
googlers797045791
pharmgkbrs797045791
gwascentralrs797045791
openSNPrs797045791
23andMers797045791
23andMe allrs797045791
SNP Nexus

SNPshotrs797045791
SNPdbers797045791
MSV3drs797045791
GWAS Ctlgrs797045791
Max Magnitude0
ClinVar
Risk rs797045791(G;G)
Alt rs797045791(G;G)
Reference rs797045791(T;T)
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.172660035A>C
CLNSRC
CLNACC RCV000192960.1,