rs1905339
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs1905339(C;C) |
Make rs1905339(C;T) |
Make rs1905339(T;T) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 17 |
Position | 42430278 |
Gene | LOC102725238 |
is a | snp |
is | mentioned by |
dbSNP | rs1905339 |
dbSNP (classic) | rs1905339 |
ClinGen | rs1905339 |
ebi | rs1905339 |
HLI | rs1905339 |
Exac | rs1905339 |
Gnomad | rs1905339 |
Varsome | rs1905339 |
LitVar | rs1905339 |
Map | rs1905339 |
PheGenI | rs1905339 |
Biobank | rs1905339 |
1000 genomes | rs1905339 |
hgdp | rs1905339 |
ensembl | rs1905339 |
geneview | rs1905339 |
scholar | rs1905339 |
rs1905339 | |
pharmgkb | rs1905339 |
gwascentral | rs1905339 |
openSNP | rs1905339 |
23andMe | rs1905339 |
SNPshot | rs1905339 |
SNPdbe | rs1905339 |
MSV3d | rs1905339 |
GWAS Ctlg | rs1905339 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 26621531] Genetic variation in the immunosuppression pathway genes and breast cancer susceptibility: a pooled analysis of 42,510 cases and 40,577 controls from the Breast Cancer Association Consortium.