Have questions? Visit https://www.reddit.com/r/SNPedia

rs796052670

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs796052670(G;T)
Make rs796052670(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome20
Position63408412
GeneKCNQ2, LOC105372724
is asnp
is mentioned by
dbSNPrs796052670
ebirs796052670
HLIrs796052670
Exacrs796052670
Varsomers796052670
Maprs796052670
PheGenIrs796052670
hapmaprs796052670
1000 genomesrs796052670
hgdprs796052670
ensemblrs796052670
gopubmedrs796052670
geneviewrs796052670
scholarrs796052670
googlers796052670
pharmgkbrs796052670
gwascentralrs796052670
openSNPrs796052670
23andMers796052670
23andMe allrs796052670
SNP Nexus

SNPshotrs796052670
SNPdbers796052670
MSV3drs796052670
GWAS Ctlgrs796052670
Max Magnitude0
ClinVar
Risk rs796052670(T;T)
Alt rs796052670(T;T)
Reference rs796052670(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene KCNQ2
CLNDBN not provided
Reversed 1
HGVS NC_000020.10:g.62039765C>A
CLNSRC
CLNACC RCV000187954.1,