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rs17667932

From SNPedia

Orientationplus
Stabilizedplus
Make rs17667932(C;C)
Make rs17667932(C;T)
Make rs17667932(T;T)
ReferenceGRCh38 38.1/141
Chromosome8
Position117537137
GeneMED30
is asnp
is mentioned by
dbSNPrs17667932
dbSNP (classic)rs17667932
ClinGenrs17667932
ebirs17667932
HLIrs17667932
Exacrs17667932
Gnomadrs17667932
Varsomers17667932
LitVarrs17667932
Maprs17667932
PheGenIrs17667932
Biobankrs17667932
1000 genomesrs17667932
hgdprs17667932
ensemblrs17667932
geneviewrs17667932
scholarrs17667932
googlers17667932
pharmgkbrs17667932
gwascentralrs17667932
openSNPrs17667932
23andMers17667932
SNPshotrs17667932
SNPdbers17667932
MSV3drs17667932
GWAS Ctlgrs17667932
GMAF0.06795
Max Magnitude0
? (C;C) (C;T) (T;T) 28


GWAS snp
PMID [PMID 22446961]
Trait
Title Two new susceptibility loci for Kawasaki disease identified through genome-wide association analysis.
Risk Allele G
P-val 5E-7
Odds Ratio 2.3680 None


[PMID 29212154OA-icon.png] Detection of susceptibility loci on APOA5 and COLEC12 associated with metabolic syndrome using a genome-wide association study in a Taiwanese population.