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rs796052675

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs796052675(C;T)
Make rs796052675(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome8
Position132180255
GeneKCNQ3
is asnp
is mentioned by
dbSNPrs796052675
ebirs796052675
HLIrs796052675
Exacrs796052675
Varsomers796052675
Maprs796052675
PheGenIrs796052675
hapmaprs796052675
1000 genomesrs796052675
hgdprs796052675
ensemblrs796052675
gopubmedrs796052675
geneviewrs796052675
scholarrs796052675
googlers796052675
pharmgkbrs796052675
gwascentralrs796052675
openSNPrs796052675
23andMers796052675
23andMe allrs796052675
SNP Nexus

SNPshotrs796052675
SNPdbers796052675
MSV3drs796052675
GWAS Ctlgrs796052675
Max Magnitude0
ClinVar
Risk rs796052675(T;T)
Alt rs796052675(T;T)
Reference rs796052675(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene KCNQ3
CLNDBN not provided
Reversed 1
HGVS NC_000008.10:g.133192502G>A
CLNSRC
CLNACC RCV000187966.1,