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

rs796052666

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs796052666(-;T)
Make rs796052666(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome20
Position63407332
GeneKCNQ2
is asnp
is mentioned by
dbSNPrs796052666
dbSNP (old)rs796052666
ClinGenrs796052666
ebirs796052666
HLIrs796052666
Exacrs796052666
Varsomers796052666
Maprs796052666
PheGenIrs796052666
Biobankrs796052666
1000 genomesrs796052666
hgdprs796052666
ensemblrs796052666
gopubmedrs796052666
geneviewrs796052666
scholarrs796052666
googlers796052666
pharmgkbrs796052666
gwascentralrs796052666
openSNPrs796052666
23andMers796052666
23andMe allrs796052666
SNP Nexus

SNPshotrs796052666
SNPdbers796052666
MSV3drs796052666
GWAS Ctlgrs796052666
Max Magnitude0
ClinVar
Risk rs796052666(T;T)
Alt rs796052666(T;T)
Reference Rs796052666(-;-)
Significance Pathogenic
Disease not provided
Variation info
Gene KCNQ2
CLNDBN not provided
Reversed 1
HGVS NC_000020.10:g.62038686dupA
CLNSRC
CLNACC RCV000187945.1,