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rs73532286

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs73532286(G;T)
Make rs73532286(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position84658286
is asnp
is mentioned by
dbSNPrs73532286
ebirs73532286
HLIrs73532286
Exacrs73532286
Varsomers73532286
Maprs73532286
PheGenIrs73532286
hapmaprs73532286
1000 genomesrs73532286
hgdprs73532286
ensemblrs73532286
gopubmedrs73532286
geneviewrs73532286
scholarrs73532286
googlers73532286
pharmgkbrs73532286
gwascentralrs73532286
openSNPrs73532286
23andMers73532286
23andMe allrs73532286
SNP Nexus

SNPshotrs73532286
SNPdbers73532286
MSV3drs73532286
GWAS Ctlgrs73532286
GMAF0.001377
Max Magnitude0

[PMID 22030984OA-icon.png] Variants in the human potassium channel gene (KCNN3) are associated with migraine in a high risk genetic isolate