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rs796052606

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs796052606(G;T)
Make rs796052606(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position160070021
GeneKCNJ10, LOC105371465
is asnp
is mentioned by
dbSNPrs796052606
ebirs796052606
HLIrs796052606
Exacrs796052606
Varsomers796052606
Maprs796052606
PheGenIrs796052606
hapmaprs796052606
1000 genomesrs796052606
hgdprs796052606
ensemblrs796052606
gopubmedrs796052606
geneviewrs796052606
scholarrs796052606
googlers796052606
pharmgkbrs796052606
gwascentralrs796052606
openSNPrs796052606
23andMers796052606
23andMe allrs796052606
SNP Nexus

SNPshotrs796052606
SNPdbers796052606
MSV3drs796052606
GWAS Ctlgrs796052606
Max Magnitude0
ClinVar
Risk rs796052606(T;T)
Alt rs796052606(T;T)
Reference rs796052606(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene KCNJ10
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.160039811C>A
CLNSRC
CLNACC RCV000187813.2,