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rs796052655

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs796052655(C;C)
Make rs796052655(C;G)
ReferenceGRCh38.p2 38.2/147
Chromosome20
Position63413479
GeneKCNQ2, LOC105372724
is asnp
is mentioned by
dbSNPrs796052655
ebirs796052655
HLIrs796052655
Exacrs796052655
Varsomers796052655
Maprs796052655
PheGenIrs796052655
hapmaprs796052655
1000 genomesrs796052655
hgdprs796052655
ensemblrs796052655
gopubmedrs796052655
geneviewrs796052655
scholarrs796052655
googlers796052655
pharmgkbrs796052655
gwascentralrs796052655
openSNPrs796052655
23andMers796052655
23andMe allrs796052655
SNP Nexus

SNPshotrs796052655
SNPdbers796052655
MSV3drs796052655
GWAS Ctlgrs796052655
Max Magnitude0
ClinVar
Risk rs796052655(C;C)
Alt rs796052655(C;C)
Reference rs796052655(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene KCNQ2
CLNDBN not provided
Reversed 1
HGVS NC_000020.10:g.62044832C>G
CLNSRC
CLNACC RCV000187919.2,