rs281865417
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs281865417(A;A) |
Make rs281865417(A;G) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | MT |
Position | 6277 |
Gene | COX1 |
is a | snp |
is | mentioned by |
dbSNP | rs281865417 |
dbSNP (classic) | rs281865417 |
ClinGen | rs281865417 |
ebi | rs281865417 |
HLI | rs281865417 |
Exac | rs281865417 |
Gnomad | rs281865417 |
Varsome | rs281865417 |
LitVar | rs281865417 |
Map | rs281865417 |
PheGenI | rs281865417 |
Biobank | rs281865417 |
1000 genomes | rs281865417 |
hgdp | rs281865417 |
ensembl | rs281865417 |
geneview | rs281865417 |
scholar | rs281865417 |
rs281865417 | |
pharmgkb | rs281865417 |
gwascentral | rs281865417 |
openSNP | rs281865417 |
23andMe | rs281865417 |
SNPshot | rs281865417 |
SNPdbe | rs281865417 |
MSV3d | rs281865417 |
GWAS Ctlg | rs281865417 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs281865417(A;A) |
Alt | rs281865417(A;A) |
Reference | Rs281865417(G;G) |
Significance | Pathogenic |
Disease | Familial colorectal cancer |
Variation | info |
Gene | COX1 |
CLNDBN | Familial colorectal cancer |
Reversed | 0 |
HGVS | NC_012920.1:m.6277G>A |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000010310.2, |