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rs796052629

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs796052629(A;G)
Make rs796052629(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome20
Position63442530
GeneKCNQ2
is asnp
is mentioned by
dbSNPrs796052629
ebirs796052629
HLIrs796052629
Exacrs796052629
Varsomers796052629
Maprs796052629
PheGenIrs796052629
hapmaprs796052629
1000 genomesrs796052629
hgdprs796052629
ensemblrs796052629
gopubmedrs796052629
geneviewrs796052629
scholarrs796052629
googlers796052629
pharmgkbrs796052629
gwascentralrs796052629
openSNPrs796052629
23andMers796052629
23andMe allrs796052629
SNP Nexus

SNPshotrs796052629
SNPdbers796052629
MSV3drs796052629
GWAS Ctlgrs796052629
Max Magnitude0
ClinVar
Risk rs796052629(G;G)
Alt rs796052629(G;G)
Reference rs796052629(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene KCNQ2
CLNDBN not provided
Reversed 1
HGVS NC_000020.10:g.62073883T>C
CLNSRC
CLNACC RCV000187870.2,