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rs1874326

From SNPedia

Orientationplus
Stabilizedplus
Make rs1874326(A;A)
Make rs1874326(A;G)
Make rs1874326(G;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position138472645
GeneTRIM24
is asnp
is mentioned by
dbSNPrs1874326
ebirs1874326
HLIrs1874326
Exacrs1874326
Varsomers1874326
Maprs1874326
PheGenIrs1874326
hapmaprs1874326
1000 genomesrs1874326
hgdprs1874326
ensemblrs1874326
gopubmedrs1874326
geneviewrs1874326
scholarrs1874326
googlers1874326
pharmgkbrs1874326
gwascentralrs1874326
openSNPrs1874326
23andMers1874326
23andMe allrs1874326
SNP Nexus

SNPshotrs1874326
SNPdbers1874326
MSV3drs1874326
GWAS Ctlgrs1874326
GMAF0.2392
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 19197348OA-icon.png]
Trait Quantitative traits
Title Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae
Risk Allele G
P-val 0.000009
Odds Ratio 0.22 [NR] lb. increase

Weight being the quantitative trait associated with in [PMID 19197348OA-icon.png]


[PMID 20031603OA-icon.png] A genome-wide association scan of RR and QT interval duration in 3 European genetically isolated populations: the EUROSPAN project.


GET Evidence
rs1874326
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.757812
summary