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rs796052614

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs796052614(C;G)
Make rs796052614(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome20
Position63472170
GeneKCNQ2
is asnp
is mentioned by
dbSNPrs796052614
ebirs796052614
HLIrs796052614
Exacrs796052614
Varsomers796052614
Maprs796052614
PheGenIrs796052614
hapmaprs796052614
1000 genomesrs796052614
hgdprs796052614
ensemblrs796052614
gopubmedrs796052614
geneviewrs796052614
scholarrs796052614
googlers796052614
pharmgkbrs796052614
gwascentralrs796052614
openSNPrs796052614
23andMers796052614
23andMe allrs796052614
SNP Nexus

SNPshotrs796052614
SNPdbers796052614
MSV3drs796052614
GWAS Ctlgrs796052614
Max Magnitude0
ClinVar
Risk rs796052614(G;G)
Alt rs796052614(G;G)
Reference rs796052614(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene KCNQ2
CLNDBN not provided
Reversed 1
HGVS NC_000020.10:g.62103523G>C
CLNSRC
CLNACC RCV000187848.1,