Have data from 23andMe or Ancestry? Make a report automatically with Promethease !

rs1064795058

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Chromosome20
Position63438708
GeneKCNQ2
is asnp
is mentioned by
dbSNPrs1064795058
dbSNP (old)rs1064795058
ClinGenrs1064795058
ebirs1064795058
HLIrs1064795058
Exacrs1064795058
Gnomadrs1064795058
Varsomers1064795058
Maprs1064795058
PheGenIrs1064795058
Biobankrs1064795058
1000 genomesrs1064795058
hgdprs1064795058
ensemblrs1064795058
gopubmedrs1064795058
geneviewrs1064795058
scholarrs1064795058
googlers1064795058
pharmgkbrs1064795058
gwascentralrs1064795058
openSNPrs1064795058
23andMers1064795058
23andMe allrs1064795058
SNPshotrs1064795058
SNPdbers1064795058
MSV3drs1064795058
GWAS Ctlgrs1064795058
Max Magnitude0
ClinVar
Risk rs1064795058(C;C)
Alt rs1064795058(C;C)
Reference Rs1064795058(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene KCNQ2
CLNDBN not provided
Reversed 1
HGVS NC_000020.10:g.62070061A>G
CLNSRC
CLNACC RCV000484946.1,