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rs766379103

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs766379103(G;T)
Make rs766379103(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position150974830
GeneKCNH2
is asnp
is mentioned by
dbSNPrs766379103
ebirs766379103
HLIrs766379103
Exacrs766379103
Varsomers766379103
Maprs766379103
PheGenIrs766379103
hapmaprs766379103
1000 genomesrs766379103
hgdprs766379103
ensemblrs766379103
gopubmedrs766379103
geneviewrs766379103
scholarrs766379103
googlers766379103
pharmgkbrs766379103
gwascentralrs766379103
openSNPrs766379103
23andMers766379103
23andMe allrs766379103
SNP Nexus

SNPshotrs766379103
SNPdbers766379103
MSV3drs766379103
GWAS Ctlgrs766379103
Max Magnitude0
ClinVar
Risk rs766379103(T;T)
Alt rs766379103(T;T)
Reference rs766379103(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene KCNH2
CLNDBN not provided
Reversed 0
HGVS NC_000007.13:g.150671918G>T
CLNSRC
CLNACC RCV000181932.2,