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rs796052676

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs796052676(C;T)
Make rs796052676(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome8
Position132180246
GeneKCNQ3
is asnp
is mentioned by
dbSNPrs796052676
ebirs796052676
HLIrs796052676
Exacrs796052676
Varsomers796052676
Maprs796052676
PheGenIrs796052676
hapmaprs796052676
1000 genomesrs796052676
hgdprs796052676
ensemblrs796052676
gopubmedrs796052676
geneviewrs796052676
scholarrs796052676
googlers796052676
pharmgkbrs796052676
gwascentralrs796052676
openSNPrs796052676
23andMers796052676
23andMe allrs796052676
SNP Nexus

SNPshotrs796052676
SNPdbers796052676
MSV3drs796052676
GWAS Ctlgrs796052676
Max Magnitude0
ClinVar
Risk rs796052676(T;T)
Alt rs796052676(T;T)
Reference rs796052676(C;C)
Significance Probable-Pathogenic
Disease not provided Benign familial neonatal seizures 2
Variation info
Gene KCNQ3
CLNDBN not provided Benign familial neonatal seizures 2
Reversed 1
HGVS NC_000008.10:g.133192493G>A
CLNSRC
CLNACC RCV000187968.1, RCV000210407.1,