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rs786205813

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs786205813(C;C)
Make rs786205813(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position70175275
GeneKCNJ2
is asnp
is mentioned by
dbSNPrs786205813
ebirs786205813
HLIrs786205813
Exacrs786205813
Varsomers786205813
Maprs786205813
PheGenIrs786205813
hapmaprs786205813
1000 genomesrs786205813
hgdprs786205813
ensemblrs786205813
gopubmedrs786205813
geneviewrs786205813
scholarrs786205813
googlers786205813
pharmgkbrs786205813
gwascentralrs786205813
openSNPrs786205813
23andMers786205813
23andMe allrs786205813
SNP Nexus

SNPshotrs786205813
SNPdbers786205813
MSV3drs786205813
GWAS Ctlgrs786205813
Max Magnitude0
ClinVar
Risk rs786205813(C;C)
Alt rs786205813(C;C)
Reference rs786205813(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene KCNJ2
CLNDBN not provided
Reversed 0
HGVS NC_000017.10:g.68171416T>C
CLNSRC
CLNACC RCV000170975.2,