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rs796052658

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs796052658(G;T)
Make rs796052658(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome20
Position63407018
GeneKCNQ2
is asnp
is mentioned by
dbSNPrs796052658
ebirs796052658
HLIrs796052658
Exacrs796052658
Varsomers796052658
Maprs796052658
PheGenIrs796052658
hapmaprs796052658
1000 genomesrs796052658
hgdprs796052658
ensemblrs796052658
gopubmedrs796052658
geneviewrs796052658
scholarrs796052658
googlers796052658
pharmgkbrs796052658
gwascentralrs796052658
openSNPrs796052658
23andMers796052658
23andMe allrs796052658
SNP Nexus

SNPshotrs796052658
SNPdbers796052658
MSV3drs796052658
GWAS Ctlgrs796052658
Max Magnitude0
ClinVar
Risk rs796052658(T;T)
Alt rs796052658(T;T)
Reference rs796052658(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene KCNQ2
CLNDBN not provided
Reversed 1
HGVS NC_000020.10:g.62038371C>A
CLNSRC
CLNACC RCV000187933.2,