Have questions? Visit https://www.reddit.com/r/SNPedia

rs786205817

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs786205817(A;T)
Make rs786205817(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position70175935
GeneKCNJ2
is asnp
is mentioned by
dbSNPrs786205817
ebirs786205817
HLIrs786205817
Exacrs786205817
Varsomers786205817
Maprs786205817
PheGenIrs786205817
hapmaprs786205817
1000 genomesrs786205817
hgdprs786205817
ensemblrs786205817
gopubmedrs786205817
geneviewrs786205817
scholarrs786205817
googlers786205817
pharmgkbrs786205817
gwascentralrs786205817
openSNPrs786205817
23andMers786205817
23andMe allrs786205817
SNP Nexus

SNPshotrs786205817
SNPdbers786205817
MSV3drs786205817
GWAS Ctlgrs786205817
Max Magnitude0
ClinVar
Risk rs786205817(T;T)
Alt rs786205817(T;T)
Reference rs786205817(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene KCNJ2
CLNDBN not provided
Reversed 0
HGVS NC_000017.10:g.68172076A>T
CLNSRC
CLNACC RCV000170986.2,