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rs5982533

From SNPedia

Orientationplus
Stabilizedplus
Make rs5982533(C;C)
Make rs5982533(C;T)
Make rs5982533(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position112403236
GeneZCCHC16
is asnp
is mentioned by
dbSNPrs5982533
ebirs5982533
HLIrs5982533
Exacrs5982533
Varsomers5982533
Maprs5982533
PheGenIrs5982533
hapmaprs5982533
1000 genomesrs5982533
hgdprs5982533
ensemblrs5982533
gopubmedrs5982533
geneviewrs5982533
scholarrs5982533
googlers5982533
pharmgkbrs5982533
gwascentralrs5982533
openSNPrs5982533
23andMers5982533
23andMe allrs5982533
SNP Nexus

SNPshotrs5982533
SNPdbers5982533
MSV3drs5982533
GWAS Ctlgrs5982533
GMAF0.3761
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 19260141OA-icon.png]
Trait Biochemical measures
Title Genome-wide association study of biochemical traits in Korcula Island, Croatia
Risk Allele G
P-val 0.000007
Odds Ratio 0.23 [0.13-0.33] mmol/L decrease
[PMID 19260141OA-icon.png] gwas among adults residing on Korcula Island in Croatia, triglycerides, the G allele associated with decreased triglyceride levels



GET Evidence
rs5982533
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.51087
summary