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rs1064795855

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Chromosome7
Position150946952
GeneKCNH2
is asnp
is mentioned by
dbSNPrs1064795855
dbSNP (old)rs1064795855
ClinGenrs1064795855
ebirs1064795855
HLIrs1064795855
Exacrs1064795855
Gnomadrs1064795855
Varsomers1064795855
Maprs1064795855
PheGenIrs1064795855
Biobankrs1064795855
1000 genomesrs1064795855
hgdprs1064795855
ensemblrs1064795855
gopubmedrs1064795855
geneviewrs1064795855
scholarrs1064795855
googlers1064795855
pharmgkbrs1064795855
gwascentralrs1064795855
openSNPrs1064795855
23andMers1064795855
23andMe allrs1064795855
SNPshotrs1064795855
SNPdbers1064795855
MSV3drs1064795855
GWAS Ctlgrs1064795855
Max Magnitude0
ClinVar
Risk rs1064795855(-;-)
Alt rs1064795855(-;-)
Reference Rs1064795855(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene KCNH2
CLNDBN not provided
Reversed 1
HGVS NC_000007.13:g.150644040delC
CLNSRC
CLNACC RCV000481082.1,