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rs796052649

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs796052649(C;C)
Make rs796052649(C;G)
ReferenceGRCh38.p2 38.2/147
Chromosome20
Position63408537
GeneKCNQ2, LOC105372724
is asnp
is mentioned by
dbSNPrs796052649
ebirs796052649
HLIrs796052649
Exacrs796052649
Varsomers796052649
Maprs796052649
PheGenIrs796052649
hapmaprs796052649
1000 genomesrs796052649
hgdprs796052649
ensemblrs796052649
gopubmedrs796052649
geneviewrs796052649
scholarrs796052649
googlers796052649
pharmgkbrs796052649
gwascentralrs796052649
openSNPrs796052649
23andMers796052649
23andMe allrs796052649
SNP Nexus

SNPshotrs796052649
SNPdbers796052649
MSV3drs796052649
GWAS Ctlgrs796052649
Max Magnitude0
ClinVar
Risk rs796052649(C;C)
Alt rs796052649(C;C)
Reference rs796052649(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene KCNQ2
CLNDBN not provided
Reversed 1
HGVS NC_000020.10:g.62039890C>G
CLNSRC
CLNACC RCV000187909.1,