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rs786205822

From SNPedia

Orientationplus
Geno Mag Summary
(GCC;GCC) 0 common in clinvar
Make rs786205822(-;-)
Make rs786205822(-;GCC)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position70175955
GeneKCNJ2
is asnp
is mentioned by
dbSNPrs786205822
ebirs786205822
HLIrs786205822
Exacrs786205822
Varsomers786205822
Maprs786205822
PheGenIrs786205822
hapmaprs786205822
1000 genomesrs786205822
hgdprs786205822
ensemblrs786205822
gopubmedrs786205822
geneviewrs786205822
scholarrs786205822
googlers786205822
pharmgkbrs786205822
gwascentralrs786205822
openSNPrs786205822
23andMers786205822
23andMe allrs786205822
SNP Nexus

SNPshotrs786205822
SNPdbers786205822
MSV3drs786205822
GWAS Ctlgrs786205822
Max Magnitude0
ClinVar
Risk rs786205822(;)
Alt rs786205822(;)
Reference rs786205822(GCC;GCC)
Significance Probable-Pathogenic
Disease Cardiac arrhythmia
Variation info
Gene KCNJ2
CLNDBN Cardiac arrhythmia
Reversed 0
HGVS NC_000017.10:g.68172096_68172098delGCC
CLNSRC
CLNACC RCV000170997.2,