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rs796052621

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs796052621(A;A)
Make rs796052621(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome20
Position63444756
GeneKCNQ2
is asnp
is mentioned by
dbSNPrs796052621
ebirs796052621
HLIrs796052621
Exacrs796052621
Varsomers796052621
Maprs796052621
PheGenIrs796052621
hapmaprs796052621
1000 genomesrs796052621
hgdprs796052621
ensemblrs796052621
gopubmedrs796052621
geneviewrs796052621
scholarrs796052621
googlers796052621
pharmgkbrs796052621
gwascentralrs796052621
openSNPrs796052621
23andMers796052621
23andMe allrs796052621
SNP Nexus

SNPshotrs796052621
SNPdbers796052621
MSV3drs796052621
GWAS Ctlgrs796052621
Max Magnitude0
ClinVar
Risk rs796052621(A;A)
Alt rs796052621(A;A)
Reference rs796052621(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene KCNQ2
CLNDBN not provided
Reversed 1
HGVS NC_000020.10:g.62076109C>T
CLNSRC
CLNACC RCV000187856.2,