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rs765427343

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs765427343(A;C)
Make rs765427343(C;C)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position150948471
GeneKCNH2
is asnp
is mentioned by
dbSNPrs765427343
ebirs765427343
HLIrs765427343
Exacrs765427343
Varsomers765427343
Maprs765427343
PheGenIrs765427343
hapmaprs765427343
1000 genomesrs765427343
hgdprs765427343
ensemblrs765427343
gopubmedrs765427343
geneviewrs765427343
scholarrs765427343
googlers765427343
pharmgkbrs765427343
gwascentralrs765427343
openSNPrs765427343
23andMers765427343
23andMe allrs765427343
SNP Nexus

SNPshotrs765427343
SNPdbers765427343
MSV3drs765427343
GWAS Ctlgrs765427343
Max Magnitude0
ClinVar
Risk rs765427343(C,T;C,T)
Alt rs765427343(C,T;C,T)
Reference rs765427343(A;A)
Significance Probable-Pathogenic
Disease Cardiac arrhythmia
Variation info
Gene KCNH2
CLNDBN Cardiac arrhythmia
Reversed 0
HGVS NC_000007.13:g.150645559A>C
CLNSRC
CLNACC RCV000181878.1,