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rs796052625

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs796052625(C;C)
Make rs796052625(C;G)
ReferenceGRCh38.p2 38.2/147
Chromosome20
Position63444737
GeneKCNQ2
is asnp
is mentioned by
dbSNPrs796052625
ebirs796052625
HLIrs796052625
Exacrs796052625
Varsomers796052625
Maprs796052625
PheGenIrs796052625
hapmaprs796052625
1000 genomesrs796052625
hgdprs796052625
ensemblrs796052625
gopubmedrs796052625
geneviewrs796052625
scholarrs796052625
googlers796052625
pharmgkbrs796052625
gwascentralrs796052625
openSNPrs796052625
23andMers796052625
23andMe allrs796052625
SNP Nexus

SNPshotrs796052625
SNPdbers796052625
MSV3drs796052625
GWAS Ctlgrs796052625
Max Magnitude0
ClinVar
Risk rs796052625(C,T;C,T)
Alt rs796052625(C,T;C,T)
Reference rs796052625(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene KCNQ2
CLNDBN not provided
Reversed 1
HGVS NC_000020.10:g.62076090C>A; NC_000020.10:g.62076090C>G
CLNSRC
CLNACC RCV000187861.2, RCV000187860.2,