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rs796052664

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(TC;TC) 0 common in clinvar
Make rs796052664(CCT;CCT)
Make rs796052664(CCT;TC)
ReferenceGRCh38.p2 38.2/147
Chromosome20
Position63439649
GeneKCNQ2
is asnp
is mentioned by
dbSNPrs796052664
dbSNP (old)rs796052664
ClinGenrs796052664
ebirs796052664
HLIrs796052664
Exacrs796052664
Gnomadrs796052664
Varsomers796052664
Maprs796052664
PheGenIrs796052664
Biobankrs796052664
1000 genomesrs796052664
hgdprs796052664
ensemblrs796052664
gopubmedrs796052664
geneviewrs796052664
scholarrs796052664
googlers796052664
pharmgkbrs796052664
gwascentralrs796052664
openSNPrs796052664
23andMers796052664
23andMe allrs796052664
SNP Nexus

SNPshotrs796052664
SNPdbers796052664
MSV3drs796052664
GWAS Ctlgrs796052664
Max Magnitude0
ClinVar
Risk rs796052664(CCT;CCT)
Alt rs796052664(CCT;CCT)
Reference Rs796052664(TC;TC)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene KCNQ2
CLNDBN not provided
Reversed 1
HGVS NC_000020.10:g.62071002_62071003delGAinsAGG
CLNSRC
CLNACC RCV000187943.1,