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rs864321649

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs864321649(A;A)
Make rs864321649(A;C)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position173233101
GeneNKX2-5
is asnp
is mentioned by
dbSNPrs864321649
ebirs864321649
HLIrs864321649
Exacrs864321649
Varsomers864321649
Maprs864321649
PheGenIrs864321649
hapmaprs864321649
1000 genomesrs864321649
hgdprs864321649
ensemblrs864321649
gopubmedrs864321649
geneviewrs864321649
scholarrs864321649
googlers864321649
pharmgkbrs864321649
gwascentralrs864321649
openSNPrs864321649
23andMers864321649
23andMe allrs864321649
SNP Nexus

SNPshotrs864321649
SNPdbers864321649
MSV3drs864321649
GWAS Ctlgrs864321649
Max Magnitude0
ClinVar
Risk rs864321649(A;A)
Alt rs864321649(A;A)
Reference rs864321649(C;C)
Significance Pathogenic
Disease Congenital heart disease
Variation info
Gene NKX2-5
CLNDBN Congenital heart disease
Reversed 1
HGVS NC_000005.9:g.172660104G>T
CLNSRC
CLNACC RCV000203525.1,