rs587776622
From SNPedia
Orientation | plus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
(G;G) | 0 | common in clinvar |
Make rs587776622(A;A) |
Make rs587776622(A;C) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 14 |
Position | 75047174 |
Gene | MLH3 |
is a | snp |
is | mentioned by |
dbSNP | rs587776622 |
dbSNP (classic) | rs587776622 |
ClinGen | rs587776622 |
ebi | rs587776622 |
HLI | rs587776622 |
Exac | rs587776622 |
Gnomad | rs587776622 |
Varsome | rs587776622 |
LitVar | rs587776622 |
Map | rs587776622 |
PheGenI | rs587776622 |
Biobank | rs587776622 |
1000 genomes | rs587776622 |
hgdp | rs587776622 |
ensembl | rs587776622 |
geneview | rs587776622 |
scholar | rs587776622 |
rs587776622 | |
pharmgkb | rs587776622 |
gwascentral | rs587776622 |
openSNP | rs587776622 |
23andMe | rs587776622 |
SNPshot | rs587776622 |
SNPdbe | rs587776622 |
MSV3d | rs587776622 |
GWAS Ctlg | rs587776622 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs587776622(A;A) Rs587776622(C;C) |
Alt | rs587776622(A;A) Rs587776622(C;C) |
Reference | Rs587776622(G;G) |
Significance | Pathogenic |
Disease | Carcinoma of colon |
Variation | info |
Gene | MLH3 |
CLNDBN | Carcinoma of colon |
Reversed | 1 |
HGVS | NC_000014.8:g.75513877C>A |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000005896.4, |