rs3747742
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 2 |
Make rs3747742(C;C) |
Make rs3747742(C;T) |
Make rs3747742(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 41194780 |
Gene | TREML2 |
is a | snp |
is | mentioned by |
dbSNP | rs3747742 |
dbSNP (classic) | rs3747742 |
ClinGen | rs3747742 |
ebi | rs3747742 |
HLI | rs3747742 |
Exac | rs3747742 |
Gnomad | rs3747742 |
Varsome | rs3747742 |
LitVar | rs3747742 |
Map | rs3747742 |
PheGenI | rs3747742 |
Biobank | rs3747742 |
1000 genomes | rs3747742 |
hgdp | rs3747742 |
ensembl | rs3747742 |
geneview | rs3747742 |
scholar | rs3747742 |
rs3747742 | |
pharmgkb | rs3747742 |
gwascentral | rs3747742 |
openSNP | rs3747742 |
23andMe | rs3747742 |
SNPshot | rs3747742 |
SNPdbe | rs3747742 |
MSV3d | rs3747742 |
GWAS Ctlg | rs3747742 |
Max Magnitude | 2 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
rs3747742 is a SNP in the Triggering receptor expressed on myeloid cells-like 2 TREML2 gene.
See the genotype page rs3747742(G;G).
The minor allele of rs3747742 has been reported in a large study (IGAP) to be associated with a reduced risk of Alzheimer's Disease. The protective allele is (G). The odds ratio associated with heterozygotes and homozygotes of the G allele versus the A allele is 0.93 (CI 0.89-0.96). [PMID 24439484] Missense variant in TREML2 protects against Alzheimer's disease