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rs796052678

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs796052678(C;T)
Make rs796052678(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome8
Position132175469
GeneKCNQ3
is asnp
is mentioned by
dbSNPrs796052678
ebirs796052678
HLIrs796052678
Exacrs796052678
Varsomers796052678
Maprs796052678
PheGenIrs796052678
hapmaprs796052678
1000 genomesrs796052678
hgdprs796052678
ensemblrs796052678
gopubmedrs796052678
geneviewrs796052678
scholarrs796052678
googlers796052678
pharmgkbrs796052678
gwascentralrs796052678
openSNPrs796052678
23andMers796052678
23andMe allrs796052678
SNP Nexus

SNPshotrs796052678
SNPdbers796052678
MSV3drs796052678
GWAS Ctlgrs796052678
Max Magnitude0
ClinVar
Risk rs796052678(T;T)
Alt rs796052678(T;T)
Reference rs796052678(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene KCNQ3
CLNDBN not provided
Reversed 1
HGVS NC_000008.10:g.133187716G>A
CLNSRC
CLNACC RCV000187971.2,