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rs786205811

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs786205811(C;T)
Make rs786205811(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position70175157
GeneKCNJ2
is asnp
is mentioned by
dbSNPrs786205811
ebirs786205811
HLIrs786205811
Exacrs786205811
Varsomers786205811
Maprs786205811
PheGenIrs786205811
hapmaprs786205811
1000 genomesrs786205811
hgdprs786205811
ensemblrs786205811
gopubmedrs786205811
geneviewrs786205811
scholarrs786205811
googlers786205811
pharmgkbrs786205811
gwascentralrs786205811
openSNPrs786205811
23andMers786205811
23andMe allrs786205811
SNP Nexus

SNPshotrs786205811
SNPdbers786205811
MSV3drs786205811
GWAS Ctlgrs786205811
Max Magnitude0
ClinVar
Risk rs786205811(T;T)
Alt rs786205811(T;T)
Reference rs786205811(C;C)
Significance Pathogenic
Disease not specified
Variation info
Gene KCNJ2
CLNDBN not specified
Reversed 0
HGVS NC_000017.10:g.68171298C>T
CLNSRC
CLNACC RCV000170970.3,