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rs1064793855

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Chromosome7
Position150951510
GeneKCNH2
is asnp
is mentioned by
dbSNPrs1064793855
dbSNP (old)rs1064793855
ClinGenrs1064793855
ebirs1064793855
HLIrs1064793855
Exacrs1064793855
Gnomadrs1064793855
Varsomers1064793855
Maprs1064793855
PheGenIrs1064793855
Biobankrs1064793855
1000 genomesrs1064793855
hgdprs1064793855
ensemblrs1064793855
gopubmedrs1064793855
geneviewrs1064793855
scholarrs1064793855
googlers1064793855
pharmgkbrs1064793855
gwascentralrs1064793855
openSNPrs1064793855
23andMers1064793855
23andMe allrs1064793855
SNPshotrs1064793855
SNPdbers1064793855
MSV3drs1064793855
GWAS Ctlgrs1064793855
Max Magnitude0
ClinVar
Risk rs1064793855(-;-)
Alt rs1064793855(-;-)
Reference Rs1064793855(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene KCNH2
CLNDBN not provided
Reversed 1
HGVS NC_000007.13:g.150648598delC
CLNSRC
CLNACC RCV000478962.1,