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rs876661184

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs876661184(G;G)
Make rs876661184(G;T)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position70175941
GeneKCNJ2
is asnp
is mentioned by
dbSNPrs876661184
ebirs876661184
HLIrs876661184
Exacrs876661184
Varsomers876661184
Maprs876661184
PheGenIrs876661184
hapmaprs876661184
1000 genomesrs876661184
hgdprs876661184
ensemblrs876661184
gopubmedrs876661184
geneviewrs876661184
scholarrs876661184
googlers876661184
pharmgkbrs876661184
gwascentralrs876661184
openSNPrs876661184
23andMers876661184
23andMe allrs876661184
SNP Nexus

SNPshotrs876661184
SNPdbers876661184
MSV3drs876661184
GWAS Ctlgrs876661184
Max Magnitude0
ClinVar
Risk rs876661184(G;G)
Alt rs876661184(G;G)
Reference rs876661184(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene KCNJ2
CLNDBN not provided
Reversed 0
HGVS NC_000017.10:g.68172082T>G
CLNSRC
CLNACC RCV000221740.1,