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

rs796052663

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(GT;GT) 0 common in clinvar
Make rs796052663(-;-)
Make rs796052663(-;GT)
ReferenceGRCh38.p2 38.2/147
Chromosome20
Position63446800
GeneKCNQ2, LOC105372720
is asnp
is mentioned by
dbSNPrs796052663
dbSNP (old)rs796052663
ClinGenrs796052663
ebirs796052663
HLIrs796052663
Exacrs796052663
Gnomadrs796052663
Varsomers796052663
Maprs796052663
PheGenIrs796052663
Biobankrs796052663
1000 genomesrs796052663
hgdprs796052663
ensemblrs796052663
gopubmedrs796052663
geneviewrs796052663
scholarrs796052663
googlers796052663
pharmgkbrs796052663
gwascentralrs796052663
openSNPrs796052663
23andMers796052663
23andMe allrs796052663
SNP Nexus

SNPshotrs796052663
SNPdbers796052663
MSV3drs796052663
GWAS Ctlgrs796052663
Max Magnitude0
ClinVar
Risk rs796052663(-;-)
Alt rs796052663(-;-)
Reference Rs796052663(GT;GT)
Significance Pathogenic
Disease not provided Benign familial neonatal seizures 1
Variation info
Gene KCNQ2
CLNDBN not provided Benign familial neonatal seizures 1
Reversed 1
HGVS NC_000020.10:g.62078153_62078154delAC
CLNSRC
CLNACC RCV000187942.1, RCV000408744.1,