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rs796052604

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs796052604(C;T)
Make rs796052604(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position160042312
GeneKCNJ10
is asnp
is mentioned by
dbSNPrs796052604
ebirs796052604
HLIrs796052604
Exacrs796052604
Varsomers796052604
Maprs796052604
PheGenIrs796052604
hapmaprs796052604
1000 genomesrs796052604
hgdprs796052604
ensemblrs796052604
gopubmedrs796052604
geneviewrs796052604
scholarrs796052604
googlers796052604
pharmgkbrs796052604
gwascentralrs796052604
openSNPrs796052604
23andMers796052604
23andMe allrs796052604
SNP Nexus

SNPshotrs796052604
SNPdbers796052604
MSV3drs796052604
GWAS Ctlgrs796052604
Max Magnitude0
ClinVar
Risk rs796052604(T;T)
Alt rs796052604(T;T)
Reference rs796052604(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene KCNJ10
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.160012102G>A
CLNSRC
CLNACC RCV000187806.2,