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rs2624265

From SNPedia

Orientationplus
Stabilizedplus
Make rs2624265(C;C)
Make rs2624265(C;T)
Make rs2624265(T;T)
ReferenceGRCh38 38.1/141
Chromosome15
Position38856448
is asnp
is mentioned by
dbSNPrs2624265
ebirs2624265
HLIrs2624265
Exacrs2624265
Varsomers2624265
Maprs2624265
PheGenIrs2624265
hapmaprs2624265
1000 genomesrs2624265
hgdprs2624265
ensemblrs2624265
gopubmedrs2624265
geneviewrs2624265
scholarrs2624265
googlers2624265
pharmgkbrs2624265
gwascentralrs2624265
openSNPrs2624265
23andMers2624265
23andMe allrs2624265
SNP Nexus

SNPshotrs2624265
SNPdbers2624265
MSV3drs2624265
GWAS Ctlgrs2624265
GMAF0.2603
Max Magnitude
? (C;C) (C;T) (T;T) 28
per the 23andMe blog, the minor allele of this SNP (C) was associated with increased triglycerides
SNP Rarer allele LDL HDL TG
rs6544713 T +
rs2650000 A +
rs471364 C -
rs1800961 T -
rs7679 C - +
rs2967605 T -
rs2409722 T -
rs10903129 A - - -
rs6756629 A - + -
rs12670798 C + + +
rs7395662 A - + +
rs174570 T - - +
rs2271293 A - + -
rs2624265 C +
rs2167079 T +
rs9891572 T +
rs4844614 T +
rs5031002 G +
GWAS snp
PMID [PMID 19060910OA-icon.png]
Trait Other metabolic traits
Title Genome-wide association analysis of metabolic traits in a birth cohort from a founder population
Risk Allele G
P-val 4E-7
Odds Ratio 0.07 [0.04-0.10] mmol/l increase



GET Evidence
rs2624265
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.1875
summary