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rs532891158

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs532891158(C;G)
Make rs532891158(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position150958107
GeneKCNH2
is asnp
is mentioned by
dbSNPrs532891158
ebirs532891158
HLIrs532891158
Exacrs532891158
Varsomers532891158
Maprs532891158
PheGenIrs532891158
hapmaprs532891158
1000 genomesrs532891158
hgdprs532891158
ensemblrs532891158
gopubmedrs532891158
geneviewrs532891158
scholarrs532891158
googlers532891158
pharmgkbrs532891158
gwascentralrs532891158
openSNPrs532891158
23andMers532891158
23andMe allrs532891158
SNP Nexus

SNPshotrs532891158
SNPdbers532891158
MSV3drs532891158
GWAS Ctlgrs532891158
Max Magnitude0
ClinVar
Risk rs532891158(G,T;G,T)
Alt rs532891158(G,T;G,T)
Reference rs532891158(C;C)
Significance Probable-Pathogenic
Disease not specified
Variation info
Gene KCNH2
CLNDBN not specified
Reversed 0
HGVS NC_000007.13:g.150655195C>G
CLNSRC
CLNACC RCV000181769.2,