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rs587784067

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587784067(-;-)
Make rs587784067(-;C)
ReferenceGRCh38.p2 38.2/144
Chromosome5
Position173232761
GeneNKX2-5
is asnp
is mentioned by
dbSNPrs587784067
ebirs587784067
HLIrs587784067
Exacrs587784067
Varsomers587784067
Maprs587784067
PheGenIrs587784067
hapmaprs587784067
1000 genomesrs587784067
hgdprs587784067
ensemblrs587784067
gopubmedrs587784067
geneviewrs587784067
scholarrs587784067
googlers587784067
pharmgkbrs587784067
gwascentralrs587784067
openSNPrs587784067
23andMers587784067
23andMe allrs587784067
SNP Nexus

SNPshotrs587784067
SNPdbers587784067
MSV3drs587784067
GWAS Ctlgrs587784067
Max Magnitude0
ClinVar
Risk rs587784067(;)
Alt rs587784067(;)
Reference rs587784067(C;C)
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.172659764delG
CLNSRC
CLNACC RCV000146756.1,