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rs747235713

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs747235713(C;T)
Make rs747235713(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome8
Position132129542
GeneKCNQ3
is asnp
is mentioned by
dbSNPrs747235713
ebirs747235713
HLIrs747235713
Exacrs747235713
Varsomers747235713
Maprs747235713
PheGenIrs747235713
hapmaprs747235713
1000 genomesrs747235713
hgdprs747235713
ensemblrs747235713
gopubmedrs747235713
geneviewrs747235713
scholarrs747235713
googlers747235713
pharmgkbrs747235713
gwascentralrs747235713
openSNPrs747235713
23andMers747235713
23andMe allrs747235713
SNP Nexus

SNPshotrs747235713
SNPdbers747235713
MSV3drs747235713
GWAS Ctlgrs747235713
Max Magnitude0
ClinVar
Risk rs747235713(T;T)
Alt rs747235713(T;T)
Reference rs747235713(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene KCNQ3
CLNDBN not provided
Reversed 0
HGVS NC_000008.10:g.133141789C>T
CLNSRC
CLNACC RCV000187997.1,