rs498055
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs498055(C;C) |
Make rs498055(C;T) |
Make rs498055(T;T) |
Reference | GRCh38 38.1/142 |
Chromosome | 10 |
Position | 95595157 |
Gene | RPS3AP36 |
is a | snp |
is | mentioned by |
dbSNP | rs498055 |
dbSNP (classic) | rs498055 |
ClinGen | rs498055 |
ebi | rs498055 |
HLI | rs498055 |
Exac | rs498055 |
Gnomad | rs498055 |
Varsome | rs498055 |
LitVar | rs498055 |
Map | rs498055 |
PheGenI | rs498055 |
Biobank | rs498055 |
1000 genomes | rs498055 |
hgdp | rs498055 |
ensembl | rs498055 |
geneview | rs498055 |
scholar | rs498055 |
rs498055 | |
pharmgkb | rs498055 |
gwascentral | rs498055 |
openSNP | rs498055 |
23andMe | rs498055 |
SNPshot | rs498055 |
SNPdbe | rs498055 |
MSV3d | rs498055 |
GWAS Ctlg | rs498055 |
GMAF | 0.4068 |
Max Magnitude | 0 |
rs498055 was initially suspected of being a factor in Alzheimer's disease, [PMID 16385451] but later work could not reproduce the result [PMID 16773580] [PMID 17725684].
belongs to 2 genes RPS3A and BAIAP2L1
[PMID 17000046] Lack of association of two chromosome 10q24 SNPs with Alzheimer's disease.
[PMID 18585350] A polymorphism in CALHM1 influences Ca2+ homeostasis, Abeta levels, and Alzheimer's disease risk.
[PMID 18813964] Alzheimer's disease risk variants show association with cerebrospinal fluid amyloid beta.
[PMID 18830724] Assessment of Alzheimer's disease case-control associations using family-based methods.