rs1042638
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in complete genomics |
Make rs1042638(C;T) |
Make rs1042638(T;T) |
Reference | GRCh38 38.1/142 |
Chromosome | 8 |
Position | 80037711 |
Gene | TPD52 |
is a | snp |
is | mentioned by |
dbSNP | rs1042638 |
dbSNP (classic) | rs1042638 |
ClinGen | rs1042638 |
ebi | rs1042638 |
HLI | rs1042638 |
Exac | rs1042638 |
Gnomad | rs1042638 |
Varsome | rs1042638 |
LitVar | rs1042638 |
Map | rs1042638 |
PheGenI | rs1042638 |
Biobank | rs1042638 |
1000 genomes | rs1042638 |
hgdp | rs1042638 |
ensembl | rs1042638 |
geneview | rs1042638 |
scholar | rs1042638 |
rs1042638 | |
pharmgkb | rs1042638 |
gwascentral | rs1042638 |
openSNP | rs1042638 |
23andMe | rs1042638 |
SNPshot | rs1042638 |
SNPdbe | rs1042638 |
MSV3d | rs1042638 |
GWAS Ctlg | rs1042638 |
Max Magnitude | 0 |
A valine to leucine V660L SNP at rs1042638 appears to be associated with a moderately increased risk of breast cancer. [PMID 16614108]