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rs312691

From SNPedia

Orientationplus
Stabilizedplus
Make rs312691(C;C)
Make rs312691(C;T)
Make rs312691(T;T)
ReferenceGRCh37.p5 37.3/137
Chromosome17
Position68326338
is asnp
is mentioned by
dbSNPrs312691
ebirs312691
HLIrs312691
Exacrs312691
Varsomers312691
Maprs312691
PheGenIrs312691
hapmaprs312691
1000 genomesrs312691
hgdprs312691
ensemblrs312691
gopubmedrs312691
geneviewrs312691
scholarrs312691
googlers312691
pharmgkbrs312691
gwascentralrs312691
openSNPrs312691
23andMers312691
23andMe allrs312691
SNP Nexus

SNPshotrs312691
SNPdbers312691
MSV3drs312691
GWAS Ctlgrs312691
GMAF0.3205
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 22863731]
Trait Thyrotoxic hypokalemic periodic paralysis
Title Genome-wide association study identifies a susceptibility locus for thyrotoxic periodic paralysis at 17q24.3.
Risk Allele C
P-val 8E-14
Odds Ratio 3.20 [2.40-4.40]