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rs786205820

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786205820(A;A)
Make rs786205820(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position70175974
GeneKCNJ2
is asnp
is mentioned by
dbSNPrs786205820
ebirs786205820
HLIrs786205820
Exacrs786205820
Varsomers786205820
Maprs786205820
PheGenIrs786205820
hapmaprs786205820
1000 genomesrs786205820
hgdprs786205820
ensemblrs786205820
gopubmedrs786205820
geneviewrs786205820
scholarrs786205820
googlers786205820
pharmgkbrs786205820
gwascentralrs786205820
openSNPrs786205820
23andMers786205820
23andMe allrs786205820
SNP Nexus

SNPshotrs786205820
SNPdbers786205820
MSV3drs786205820
GWAS Ctlgrs786205820
Max Magnitude0
ClinVar
Risk rs786205820(A;A)
Alt rs786205820(A;A)
Reference rs786205820(G;G)
Significance Pathogenic
Disease Cardiac arrhythmia
Variation info
Gene KCNJ2
CLNDBN Cardiac arrhythmia
Reversed 0
HGVS NC_000017.10:g.68172115G>A
CLNSRC
CLNACC RCV000170994.2,