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rs1064793832

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Chromosome7
Position150952469
GeneKCNH2
is asnp
is mentioned by
dbSNPrs1064793832
dbSNP (classic)rs1064793832
ClinGenrs1064793832
ebirs1064793832
HLIrs1064793832
Exacrs1064793832
Gnomadrs1064793832
Varsomers1064793832
LitVarrs1064793832
Maprs1064793832
PheGenIrs1064793832
Biobankrs1064793832
1000 genomesrs1064793832
hgdprs1064793832
ensemblrs1064793832
geneviewrs1064793832
scholarrs1064793832
googlers1064793832
pharmgkbrs1064793832
gwascentralrs1064793832
openSNPrs1064793832
23andMers1064793832
SNPshotrs1064793832
SNPdbers1064793832
MSV3drs1064793832
GWAS Ctlgrs1064793832
Max Magnitude0
ClinVar
Risk rs1064793832(-;-)
Alt rs1064793832(-;-)
Reference Rs1064793832(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene KCNH2
CLNDBN not provided
Reversed 1
HGVS NC_000007.13:g.150649557delC
CLNSRC
CLNACC RCV000486763.1,