rs760190301
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs760190301(-;-) |
Make rs760190301(-;T) |
Make rs760190301(T;T) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 2 |
Position | 47806587 |
Gene | FBXO11, MSH6 |
is a | snp |
is | mentioned by |
dbSNP | rs760190301 |
dbSNP (classic) | rs760190301 |
ClinGen | rs760190301 |
ebi | rs760190301 |
HLI | rs760190301 |
Exac | rs760190301 |
Gnomad | rs760190301 |
Varsome | rs760190301 |
LitVar | rs760190301 |
Map | rs760190301 |
PheGenI | rs760190301 |
Biobank | rs760190301 |
1000 genomes | rs760190301 |
hgdp | rs760190301 |
ensembl | rs760190301 |
geneview | rs760190301 |
scholar | rs760190301 |
rs760190301 | |
pharmgkb | rs760190301 |
gwascentral | rs760190301 |
openSNP | rs760190301 |
23andMe | rs760190301 |
SNPshot | rs760190301 |
SNPdbe | rs760190301 |
MSV3d | rs760190301 |
GWAS Ctlg | rs760190301 |
Max Magnitude | 0 |
Mentioned as a pathogenic/likely pathogenic mutation associated with cancer predisposition in [PMID 26681312]