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rs796052624

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs796052624(A;G)
Make rs796052624(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome20
Position63444738
GeneKCNQ2
is asnp
is mentioned by
dbSNPrs796052624
ebirs796052624
HLIrs796052624
Exacrs796052624
Varsomers796052624
Maprs796052624
PheGenIrs796052624
hapmaprs796052624
1000 genomesrs796052624
hgdprs796052624
ensemblrs796052624
gopubmedrs796052624
geneviewrs796052624
scholarrs796052624
googlers796052624
pharmgkbrs796052624
gwascentralrs796052624
openSNPrs796052624
23andMers796052624
23andMe allrs796052624
SNP Nexus

SNPshotrs796052624
SNPdbers796052624
MSV3drs796052624
GWAS Ctlgrs796052624
Max Magnitude0
ClinVar
Risk rs796052624(G;G)
Alt rs796052624(G;G)
Reference rs796052624(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene KCNQ2
CLNDBN not provided
Reversed 1
HGVS NC_000020.10:g.62076091T>C
CLNSRC
CLNACC RCV000187859.2,