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rs796052619

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs796052619(A;A)
Make rs796052619(A;C)
ReferenceGRCh38.p2 38.2/147
Chromosome20
Position63444771
GeneKCNQ2
is asnp
is mentioned by
dbSNPrs796052619
ebirs796052619
HLIrs796052619
Exacrs796052619
Varsomers796052619
Maprs796052619
PheGenIrs796052619
hapmaprs796052619
1000 genomesrs796052619
hgdprs796052619
ensemblrs796052619
gopubmedrs796052619
geneviewrs796052619
scholarrs796052619
googlers796052619
pharmgkbrs796052619
gwascentralrs796052619
openSNPrs796052619
23andMers796052619
23andMe allrs796052619
SNP Nexus

SNPshotrs796052619
SNPdbers796052619
MSV3drs796052619
GWAS Ctlgrs796052619
Max Magnitude0
ClinVar
Risk rs796052619(A;A)
Alt rs796052619(A;A)
Reference rs796052619(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene KCNQ2
CLNDBN not provided
Reversed 1
HGVS NC_000020.10:g.62076124G>T
CLNSRC
CLNACC RCV000187854.2,