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rs1064793148

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Chromosome7
Position150947679
GeneKCNH2
is asnp
is mentioned by
dbSNPrs1064793148
dbSNP (classic)rs1064793148
ClinGenrs1064793148
ebirs1064793148
HLIrs1064793148
Exacrs1064793148
Gnomadrs1064793148
Varsomers1064793148
LitVarrs1064793148
Maprs1064793148
PheGenIrs1064793148
Biobankrs1064793148
1000 genomesrs1064793148
hgdprs1064793148
ensemblrs1064793148
geneviewrs1064793148
scholarrs1064793148
googlers1064793148
pharmgkbrs1064793148
gwascentralrs1064793148
openSNPrs1064793148
23andMers1064793148
23andMe allrs1064793148
SNPshotrs1064793148
SNPdbers1064793148
MSV3drs1064793148
GWAS Ctlgrs1064793148
Max Magnitude0
ClinVar
Risk rs1064793148(-;-)
Alt rs1064793148(-;-)
Reference Rs1064793148(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene KCNH2
CLNDBN not provided
Reversed 1
HGVS NC_000007.13:g.150644767delG
CLNSRC
CLNACC RCV000482977.1,