rs141140186
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs141140186(T;T) |
Reference | GRCh38.p7 38.3/149 |
Chromosome | 13 |
Position | 52378171 |
Gene | THSD1 |
is a | snp |
is | mentioned by |
dbSNP | rs141140186 |
dbSNP (classic) | rs141140186 |
ClinGen | rs141140186 |
ebi | rs141140186 |
HLI | rs141140186 |
Exac | rs141140186 |
Gnomad | rs141140186 |
Varsome | rs141140186 |
LitVar | rs141140186 |
Map | rs141140186 |
PheGenI | rs141140186 |
Biobank | rs141140186 |
1000 genomes | rs141140186 |
hgdp | rs141140186 |
ensembl | rs141140186 |
geneview | rs141140186 |
scholar | rs141140186 |
rs141140186 | |
pharmgkb | rs141140186 |
gwascentral | rs141140186 |
openSNP | rs141140186 |
23andMe | rs141140186 |
SNPshot | rs141140186 |
SNPdbe | rs141140186 |
MSV3d | rs141140186 |
GWAS Ctlg | rs141140186 |
Max Magnitude | 0 |
This SNP represents a rare variant in the THSD1 gene on chromosome 13.
The minor allele has been reported (in heterozygotes) in a 2016 study to be potentially strongly associated with intracranial Aneurysm.[PMID 27895300]