rs121908982
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in complete genomics |
Make rs121908982(C;T) |
Make rs121908982(T;T) |
Reference | GRCh38 38.1/142 |
Chromosome | 7 |
Position | 2225526 |
Gene | MAD1L1 |
is a | snp |
is | mentioned by |
dbSNP | rs121908982 |
dbSNP (classic) | rs121908982 |
ClinGen | rs121908982 |
ebi | rs121908982 |
HLI | rs121908982 |
Exac | rs121908982 |
Gnomad | rs121908982 |
Varsome | rs121908982 |
LitVar | rs121908982 |
Map | rs121908982 |
PheGenI | rs121908982 |
Biobank | rs121908982 |
1000 genomes | rs121908982 |
hgdp | rs121908982 |
ensembl | rs121908982 |
geneview | rs121908982 |
scholar | rs121908982 |
rs121908982 | |
pharmgkb | rs121908982 |
gwascentral | rs121908982 |
openSNP | rs121908982 |
23andMe | rs121908982 |
SNPshot | rs121908982 |
SNPdbe | rs121908982 |
MSV3d | rs121908982 |
GWAS Ctlg | rs121908982 |
Merged from | Rs28939694 |
GMAF | 0.0009183 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs121908982(T;T) |
Alt | rs121908982(T;T) |
Reference | Rs121908982(C;C) |
Significance | Pathogenic |
Disease | Prostate cancer |
Variation | info |
Gene | MAD1L1 |
CLNDBN | Prostate cancer, somatic |
Reversed | 1 |
HGVS | NC_000007.13:g.2265161G>A |
CLNSRC | OMIM Allelic Variant UniProtKB (protein) |
CLNACC | RCV000007329.4, |