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rs754896169

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs754896169(C;T)
Make rs754896169(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome8
Position132129530
GeneKCNQ3
is asnp
is mentioned by
dbSNPrs754896169
ebirs754896169
HLIrs754896169
Exacrs754896169
Varsomers754896169
Maprs754896169
PheGenIrs754896169
hapmaprs754896169
1000 genomesrs754896169
hgdprs754896169
ensemblrs754896169
gopubmedrs754896169
geneviewrs754896169
scholarrs754896169
googlers754896169
pharmgkbrs754896169
gwascentralrs754896169
openSNPrs754896169
23andMers754896169
23andMe allrs754896169
SNP Nexus

SNPshotrs754896169
SNPdbers754896169
MSV3drs754896169
GWAS Ctlgrs754896169
Max Magnitude0
ClinVar
Risk rs754896169(T;T)
Alt rs754896169(T;T)
Reference rs754896169(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene KCNQ3
CLNDBN not provided
Reversed 0
HGVS NC_000008.10:g.133141777C>T
CLNSRC
CLNACC RCV000187998.1,