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rs876661380

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs876661380(G;T)
Make rs876661380(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome5
Position173234749
GeneNKX2-5
is asnp
is mentioned by
dbSNPrs876661380
ebirs876661380
HLIrs876661380
Exacrs876661380
Varsomers876661380
Maprs876661380
PheGenIrs876661380
hapmaprs876661380
1000 genomesrs876661380
hgdprs876661380
ensemblrs876661380
gopubmedrs876661380
geneviewrs876661380
scholarrs876661380
googlers876661380
pharmgkbrs876661380
gwascentralrs876661380
openSNPrs876661380
23andMers876661380
23andMe allrs876661380
SNP Nexus

SNPshotrs876661380
SNPdbers876661380
MSV3drs876661380
GWAS Ctlgrs876661380
Max Magnitude0
ClinVar
Risk rs876661380(T;T)
Alt rs876661380(T;T)
Reference rs876661380(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene NKX2-5
CLNDBN not provided
Reversed 1
HGVS NC_000005.9:g.172661752C>A
CLNSRC
CLNACC RCV000223896.1,