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rs786205818

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs786205818(A;G)
Make rs786205818(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position70175940
GeneKCNJ2
is asnp
is mentioned by
dbSNPrs786205818
ebirs786205818
HLIrs786205818
Exacrs786205818
Varsomers786205818
Maprs786205818
PheGenIrs786205818
hapmaprs786205818
1000 genomesrs786205818
hgdprs786205818
ensemblrs786205818
gopubmedrs786205818
geneviewrs786205818
scholarrs786205818
googlers786205818
pharmgkbrs786205818
gwascentralrs786205818
openSNPrs786205818
23andMers786205818
23andMe allrs786205818
SNP Nexus

SNPshotrs786205818
SNPdbers786205818
MSV3drs786205818
GWAS Ctlgrs786205818
Max Magnitude0
ClinVar
Risk rs786205818(G;G)
Alt rs786205818(G;G)
Reference rs786205818(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene KCNJ2
CLNDBN not provided
Reversed 0
HGVS NC_000017.10:g.68172081A>G
CLNSRC
CLNACC RCV000170988.2,