rs228595
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs228595(A;A) |
Make rs228595(A;G) |
Make rs228595(G;G) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 11 |
Position | 108234866 |
Gene | ATM |
is a | snp |
is | mentioned by |
dbSNP | rs228595 |
dbSNP (classic) | rs228595 |
ClinGen | rs228595 |
ebi | rs228595 |
HLI | rs228595 |
Exac | rs228595 |
Gnomad | rs228595 |
Varsome | rs228595 |
LitVar | rs228595 |
Map | rs228595 |
PheGenI | rs228595 |
Biobank | rs228595 |
1000 genomes | rs228595 |
hgdp | rs228595 |
ensembl | rs228595 |
geneview | rs228595 |
scholar | rs228595 |
rs228595 | |
pharmgkb | rs228595 |
gwascentral | rs228595 |
openSNP | rs228595 |
23andMe | rs228595 |
SNPshot | rs228595 |
SNPdbe | rs228595 |
MSV3d | rs228595 |
GWAS Ctlg | rs228595 |
Max Magnitude | 0 |
[PMID 27796716] Association of breast cancer risk in BRCA1 and BRCA2 mutation carriers with genetic variants showing differential allelic expression: identification of a modifier of breast cancer risk at locus 11q22.3.