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rs876661381

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs876661381(-;-)
Make rs876661381(-;C)
ReferenceGRCh38.p2 38.2/147
Chromosome5
Position173233101
GeneNKX2-5
is asnp
is mentioned by
dbSNPrs876661381
ebirs876661381
HLIrs876661381
Exacrs876661381
Varsomers876661381
Maprs876661381
PheGenIrs876661381
hapmaprs876661381
1000 genomesrs876661381
hgdprs876661381
ensemblrs876661381
gopubmedrs876661381
geneviewrs876661381
scholarrs876661381
googlers876661381
pharmgkbrs876661381
gwascentralrs876661381
openSNPrs876661381
23andMers876661381
23andMe allrs876661381
SNP Nexus

SNPshotrs876661381
SNPdbers876661381
MSV3drs876661381
GWAS Ctlgrs876661381
Max Magnitude0
ClinVar
Risk rs876661381(;)
Alt rs876661381(;)
Reference rs876661381(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene NKX2-5
CLNDBN not provided
Reversed 1
HGVS NC_000005.9:g.172660104delG
CLNSRC
CLNACC RCV000223727.1,