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rs1064796584

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(CG;CG) 0 common in clinvar
Chromosome7
Position150950938
GeneKCNH2
is asnp
is mentioned by
dbSNPrs1064796584
dbSNP (classic)rs1064796584
ClinGenrs1064796584
ebirs1064796584
HLIrs1064796584
Exacrs1064796584
Gnomadrs1064796584
Varsomers1064796584
LitVarrs1064796584
Maprs1064796584
PheGenIrs1064796584
Biobankrs1064796584
1000 genomesrs1064796584
hgdprs1064796584
ensemblrs1064796584
geneviewrs1064796584
scholarrs1064796584
googlers1064796584
pharmgkbrs1064796584
gwascentralrs1064796584
openSNPrs1064796584
23andMers1064796584
SNPshotrs1064796584
SNPdbers1064796584
MSV3drs1064796584
GWAS Ctlgrs1064796584
Max Magnitude0
ClinVar
Risk rs1064796584(-;-)
Alt rs1064796584(-;-)
Reference Rs1064796584(CG;CG)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene KCNH2
CLNDBN not provided
Reversed 1
HGVS NC_000007.13:g.150648026_150648027delCG
CLNSRC
CLNACC RCV000487074.1,