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rs2075292

From SNPedia

Orientationplus
Stabilizedplus
Make rs2075292(G;G)
Make rs2075292(G;T)
Make rs2075292(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position116861796
GeneSIK3
is asnp
is mentioned by
dbSNPrs2075292
ebirs2075292
HLIrs2075292
Exacrs2075292
Varsomers2075292
Maprs2075292
PheGenIrs2075292
hapmaprs2075292
1000 genomesrs2075292
hgdprs2075292
ensemblrs2075292
gopubmedrs2075292
geneviewrs2075292
scholarrs2075292
googlers2075292
pharmgkbrs2075292
gwascentralrs2075292
openSNPrs2075292
23andMers2075292
23andMe allrs2075292
SNP Nexus

SNPshotrs2075292
SNPdbers2075292
MSV3drs2075292
GWAS Ctlgrs2075292
GMAF0.2401
Max Magnitude
? (G;G) (G;T) (T;T) 28
GWAS snp
PMID [PMID 18193046]
Trait Triglycerides
Title Genome-wide scan identifies variation in MLXIPL associated with plasma triglycerides
Risk Allele G
P-val 4.9999999999999998E-8
Odds Ratio 8.70 [5.76-11.64] % higher


GET Evidence
rs2075292
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.894125
summary