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rs623011

From SNPedia

Orientationplus
Stabilizedplus
Make rs623011(A;A)
Make rs623011(A;G)
Make rs623011(G;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position70263305
is asnp
is mentioned by
dbSNPrs623011
ebirs623011
HLIrs623011
Exacrs623011
Varsomers623011
Maprs623011
PheGenIrs623011
hapmaprs623011
1000 genomesrs623011
hgdprs623011
ensemblrs623011
gopubmedrs623011
geneviewrs623011
scholarrs623011
googlers623011
pharmgkbrs623011
gwascentralrs623011
openSNPrs623011
23andMers623011
23andMe allrs623011
SNP Nexus

SNPshotrs623011
SNPdbers623011
MSV3drs623011
GWAS Ctlgrs623011
GMAF0.3398
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 22399142]
Trait
Title A genome-wide association study identifies novel susceptibility genetic variation for thyrotoxic hypokalemic periodic paralysis.
Risk Allele A
P-val 4E-12
Odds Ratio 5.4700 None


[PMID 22910584] Genetic variant rs623011 (17q24.3) associates with non-familial thyrotoxic and sporadic hypokalemic paralysis.