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rs796052633

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs796052633(G;T)
Make rs796052633(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome20
Position63442416
GeneKCNQ2
is asnp
is mentioned by
dbSNPrs796052633
ebirs796052633
HLIrs796052633
Exacrs796052633
Varsomers796052633
Maprs796052633
PheGenIrs796052633
hapmaprs796052633
1000 genomesrs796052633
hgdprs796052633
ensemblrs796052633
gopubmedrs796052633
geneviewrs796052633
scholarrs796052633
googlers796052633
pharmgkbrs796052633
gwascentralrs796052633
openSNPrs796052633
23andMers796052633
23andMe allrs796052633
SNP Nexus

SNPshotrs796052633
SNPdbers796052633
MSV3drs796052633
GWAS Ctlgrs796052633
Max Magnitude0
ClinVar
Risk rs796052633(T;T)
Alt rs796052633(T;T)
Reference rs796052633(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene KCNQ2
CLNDBN not provided
Reversed 1
HGVS NC_000020.10:g.62073769C>A
CLNSRC
CLNACC RCV000187876.2,