rs121909055
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs121909055(A;A) |
Make rs121909055(A;C) |
Reference | GRCh38 38.1/141 |
Chromosome | 2 |
Position | 110658451 |
Gene | BUB1, SNORD132 |
is a | snp |
is | mentioned by |
dbSNP | rs121909055 |
dbSNP (classic) | rs121909055 |
ClinGen | rs121909055 |
ebi | rs121909055 |
HLI | rs121909055 |
Exac | rs121909055 |
Gnomad | rs121909055 |
Varsome | rs121909055 |
LitVar | rs121909055 |
Map | rs121909055 |
PheGenI | rs121909055 |
Biobank | rs121909055 |
1000 genomes | rs121909055 |
hgdp | rs121909055 |
ensembl | rs121909055 |
geneview | rs121909055 |
scholar | rs121909055 |
rs121909055 | |
pharmgkb | rs121909055 |
gwascentral | rs121909055 |
openSNP | rs121909055 |
23andMe | rs121909055 |
SNPshot | rs121909055 |
SNPdbe | rs121909055 |
MSV3d | rs121909055 |
GWAS Ctlg | rs121909055 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs121909055(A;A) |
Alt | rs121909055(A;A) |
Reference | Rs121909055(C;C) |
Significance | Pathogenic |
Disease | Colorectal cancer with chromosomal instability |
Variation | info |
Gene | BUB1 SNORD132 |
CLNDBN | Colorectal cancer with chromosomal instability |
Reversed | 1 |
HGVS | NC_000002.11:g.111416028G>T |
CLNSRC | OMIM Allelic Variant UniProtKB (protein) |
CLNACC | RCV000007499.2, |