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

rs796052657

From SNPedia

Orientationminus
Make rs796052657(-;-)
Make rs796052657(-;C)
ReferenceGRCh38.p2 38.2/147
Chromosome20
Position63428424
GeneKCNQ2
is asnp
is mentioned by
dbSNPrs796052657
ebirs796052657
HLIrs796052657
Exacrs796052657
Varsomers796052657
Maprs796052657
PheGenIrs796052657
hapmaprs796052657
1000 genomesrs796052657
hgdprs796052657
ensemblrs796052657
gopubmedrs796052657
geneviewrs796052657
scholarrs796052657
googlers796052657
pharmgkbrs796052657
gwascentralrs796052657
openSNPrs796052657
23andMers796052657
23andMe allrs796052657
SNP Nexus

SNPshotrs796052657
SNPdbers796052657
MSV3drs796052657
GWAS Ctlgrs796052657
Max Magnitude
ClinVar
Risk rs796052657(;)
Alt rs796052657(;)
Reference rs796052657(C;C)
Significance Pathogenic
Disease not provided Early infantile epileptic encephalopathy
Variation info
Gene KCNQ2
CLNDBN not provided Early infantile epileptic encephalopathy
Reversed 1
HGVS NC_000020.10:g.62059777delG
CLNSRC
CLNACC RCV000187931.1, RCV000226746.1,