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rs781247868

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs781247868(A;A)
Make rs781247868(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position150974752
GeneKCNH2
is asnp
is mentioned by
dbSNPrs781247868
ebirs781247868
HLIrs781247868
Exacrs781247868
Varsomers781247868
Maprs781247868
PheGenIrs781247868
hapmaprs781247868
1000 genomesrs781247868
hgdprs781247868
ensemblrs781247868
gopubmedrs781247868
geneviewrs781247868
scholarrs781247868
googlers781247868
pharmgkbrs781247868
gwascentralrs781247868
openSNPrs781247868
23andMers781247868
23andMe allrs781247868
SNP Nexus

SNPshotrs781247868
SNPdbers781247868
MSV3drs781247868
GWAS Ctlgrs781247868
Max Magnitude0
ClinVar
Risk rs781247868(A,C;A,C)
Alt rs781247868(A,C;A,C)
Reference rs781247868(G;G)
Significance Probable-Pathogenic
Disease Cardiac arrhythmia
Variation info
Gene KCNH2
CLNDBN Cardiac arrhythmia
Reversed 0
HGVS NC_000007.13:g.150671840G>A
CLNSRC
CLNACC RCV000181941.1,