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rs368507376

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs368507376(A;A)
Make rs368507376(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position2587583
GeneKCNQ1
is asnp
is mentioned by
dbSNPrs368507376
ebirs368507376
HLIrs368507376
Exacrs368507376
Varsomers368507376
Maprs368507376
PheGenIrs368507376
hapmaprs368507376
1000 genomesrs368507376
hgdprs368507376
ensemblrs368507376
gopubmedrs368507376
geneviewrs368507376
scholarrs368507376
googlers368507376
pharmgkbrs368507376
gwascentralrs368507376
openSNPrs368507376
23andMers368507376
23andMe allrs368507376
SNP Nexus

SNPshotrs368507376
SNPdbers368507376
MSV3drs368507376
GWAS Ctlgrs368507376
Max Magnitude0
ClinVar
Risk rs368507376(A;A)
Alt rs368507376(A;A)
Reference rs368507376(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene KCNQ1
CLNDBN not provided
Reversed 0
HGVS NC_000011.9:g.2608813G>A
CLNSRC
CLNACC RCV000182180.1,