rs28930073
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 |
Make rs28930073(C;C) |
Make rs28930073(C;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 3 |
Position | 37007004 |
Gene | MLH1 |
is a | snp |
is | mentioned by |
dbSNP | rs28930073 |
dbSNP (classic) | rs28930073 |
ClinGen | rs28930073 |
ebi | rs28930073 |
HLI | rs28930073 |
Exac | rs28930073 |
Gnomad | rs28930073 |
Varsome | rs28930073 |
LitVar | rs28930073 |
Map | rs28930073 |
PheGenI | rs28930073 |
Biobank | rs28930073 |
1000 genomes | rs28930073 |
hgdp | rs28930073 |
ensembl | rs28930073 |
geneview | rs28930073 |
scholar | rs28930073 |
rs28930073 | |
pharmgkb | rs28930073 |
gwascentral | rs28930073 |
openSNP | rs28930073 |
23andMe | rs28930073 |
SNPshot | rs28930073 |
SNPdbe | rs28930073 |
MSV3d | rs28930073 |
GWAS Ctlg | rs28930073 |
Merged from | Rs121912963 |
Max Magnitude | 0 |
[PMID 19665066] A MLH1 polymorphism that increases cancer risk is associated with better outcome in sporadic colorectal cancer
ClinVar | |
---|---|
Risk | rs28930073(C;C) |
Alt | rs28930073(C;C) |
Reference | Rs28930073(G;G) |
Significance | Other |
Disease | Colorectal cancer Lynch syndrome Hereditary cancer-predisposing syndrome not specified |
Variation | info |
Gene | MLH1 |
CLNDBN | Colorectal cancer, sporadic, susceptibility to Lynch syndrome Hereditary cancer-predisposing syndrome not specified |
Reversed | 0 |
HGVS | NC_000003.11:g.37048495G>C |
CLNSRC | OMIM Allelic Variant UniProtKB (protein) |
CLNACC | RCV000018628.2, RCV000075697.5, RCV000115482.7, RCV000200983.3, |