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rs143072395

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs143072395(A;A)
Make rs143072395(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position150950366
GeneKCNH2
is asnp
is mentioned by
dbSNPrs143072395
ebirs143072395
HLIrs143072395
Exacrs143072395
Varsomers143072395
Maprs143072395
PheGenIrs143072395
hapmaprs143072395
1000 genomesrs143072395
hgdprs143072395
ensemblrs143072395
gopubmedrs143072395
geneviewrs143072395
scholarrs143072395
googlers143072395
pharmgkbrs143072395
gwascentralrs143072395
openSNPrs143072395
23andMers143072395
23andMe allrs143072395
SNP Nexus

SNPshotrs143072395
SNPdbers143072395
MSV3drs143072395
GWAS Ctlgrs143072395
Max Magnitude0
ClinVar
Risk rs143072395(A;A)
Alt rs143072395(A;A)
Reference rs143072395(G;G)
Significance Probable-Pathogenic
Disease not specified
Variation info
Gene KCNH2
CLNDBN not specified
Reversed 0
HGVS NC_000007.13:g.150647454G>A
CLNSRC
CLNACC RCV000182043.2,