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rs864321645

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs864321645(G;T)
Make rs864321645(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position173233210
GeneNKX2-5
is asnp
is mentioned by
dbSNPrs864321645
ebirs864321645
HLIrs864321645
Exacrs864321645
Varsomers864321645
Maprs864321645
PheGenIrs864321645
hapmaprs864321645
1000 genomesrs864321645
hgdprs864321645
ensemblrs864321645
gopubmedrs864321645
geneviewrs864321645
scholarrs864321645
googlers864321645
pharmgkbrs864321645
gwascentralrs864321645
openSNPrs864321645
23andMers864321645
23andMe allrs864321645
SNP Nexus

SNPshotrs864321645
SNPdbers864321645
MSV3drs864321645
GWAS Ctlgrs864321645
Max Magnitude0
ClinVar
Risk rs864321645(T;T)
Alt rs864321645(T;T)
Reference rs864321645(G;G)
Significance Pathogenic
Disease Congenital heart disease
Variation info
Gene NKX2-5
CLNDBN Congenital heart disease
Reversed 1
HGVS NC_000005.9:g.172660213C>A
CLNSRC
CLNACC RCV000203558.1,