rs139709573
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;G) | 5 | Possible link to late-onset Alzheimer's, at least in Icelanders |
(G;G) | 0 | common/normal |
Make rs139709573(A;A) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 15 |
Position | 101646763 |
Gene | TM2D3 |
is a | snp |
is | mentioned by |
dbSNP | rs139709573 |
dbSNP (classic) | rs139709573 |
ClinGen | rs139709573 |
ebi | rs139709573 |
HLI | rs139709573 |
Exac | rs139709573 |
Gnomad | rs139709573 |
Varsome | rs139709573 |
LitVar | rs139709573 |
Map | rs139709573 |
PheGenI | rs139709573 |
Biobank | rs139709573 |
1000 genomes | rs139709573 |
hgdp | rs139709573 |
ensembl | rs139709573 |
geneview | rs139709573 |
scholar | rs139709573 |
rs139709573 | |
pharmgkb | rs139709573 |
gwascentral | rs139709573 |
openSNP | rs139709573 |
23andMe | rs139709573 |
SNPshot | rs139709573 |
SNPdbe | rs139709573 |
MSV3d | rs139709573 |
GWAS Ctlg | rs139709573 |
Max Magnitude | 5 |
rs139709573, also known as Pro155Leu or P155L, is a rare variant in the TM2D3 gene on chromosome 15.
At least in Icelanders, although not proven statistically for other Europeans (where it's ten-fold rarer), the rare rs139709573(A) allele was associated with increased risk and earlier onset of late-onset Alzheimer's disease, with an odds ratio of 7.5 (CI:3.5–15.9), p = 6.6x10e-9.[1]