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rs796052631

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs796052631(C;C)
Make rs796052631(C;T)
ReferenceGRCh38.p2 38.2/147
Chromosome20
Position63442440
GeneKCNQ2
is asnp
is mentioned by
dbSNPrs796052631
ebirs796052631
HLIrs796052631
Exacrs796052631
Varsomers796052631
Maprs796052631
PheGenIrs796052631
hapmaprs796052631
1000 genomesrs796052631
hgdprs796052631
ensemblrs796052631
gopubmedrs796052631
geneviewrs796052631
scholarrs796052631
googlers796052631
pharmgkbrs796052631
gwascentralrs796052631
openSNPrs796052631
23andMers796052631
23andMe allrs796052631
SNP Nexus

SNPshotrs796052631
SNPdbers796052631
MSV3drs796052631
GWAS Ctlgrs796052631
Max Magnitude0
ClinVar
Risk rs796052631(C;C)
Alt rs796052631(C;C)
Reference rs796052631(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene KCNQ2
CLNDBN not provided
Reversed 1
HGVS NC_000020.10:g.62073793A>G
CLNSRC
CLNACC RCV000187873.1,