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rs771674303

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs771674303(A;A)
Make rs771674303(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position150950240
GeneKCNH2
is asnp
is mentioned by
dbSNPrs771674303
ebirs771674303
HLIrs771674303
Exacrs771674303
Varsomers771674303
Maprs771674303
PheGenIrs771674303
hapmaprs771674303
1000 genomesrs771674303
hgdprs771674303
ensemblrs771674303
gopubmedrs771674303
geneviewrs771674303
scholarrs771674303
googlers771674303
pharmgkbrs771674303
gwascentralrs771674303
openSNPrs771674303
23andMers771674303
23andMe allrs771674303
SNP Nexus

SNPshotrs771674303
SNPdbers771674303
MSV3drs771674303
GWAS Ctlgrs771674303
Max Magnitude0
ClinVar
Risk rs771674303(A,T;A,T)
Alt rs771674303(A,T;A,T)
Reference rs771674303(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene KCNH2
CLNDBN not provided
Reversed 0
HGVS NC_000007.13:g.150647328G>A
CLNSRC
CLNACC RCV000181847.1,