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rs796052641

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs796052641(C;T)
Make rs796052641(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome20
Position63438644
GeneKCNQ2
is asnp
is mentioned by
dbSNPrs796052641
ebirs796052641
HLIrs796052641
Exacrs796052641
Varsomers796052641
Maprs796052641
PheGenIrs796052641
hapmaprs796052641
1000 genomesrs796052641
hgdprs796052641
ensemblrs796052641
gopubmedrs796052641
geneviewrs796052641
scholarrs796052641
googlers796052641
pharmgkbrs796052641
gwascentralrs796052641
openSNPrs796052641
23andMers796052641
23andMe allrs796052641
SNP Nexus

SNPshotrs796052641
SNPdbers796052641
MSV3drs796052641
GWAS Ctlgrs796052641
Max Magnitude0
ClinVar
Risk rs796052641(T;T)
Alt rs796052641(T;T)
Reference rs796052641(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene KCNQ2
CLNDBN not provided
Reversed 1
HGVS NC_000020.10:g.62069997G>A
CLNSRC
CLNACC RCV000187889.1,