rs34126013
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs34126013(C;T) |
Make rs34126013(T;T) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 1 |
Position | 45332458 |
Gene | MUTYH |
is a | snp |
is | mentioned by |
dbSNP | rs34126013 |
dbSNP (classic) | rs34126013 |
ClinGen | rs34126013 |
ebi | rs34126013 |
HLI | rs34126013 |
Exac | rs34126013 |
Gnomad | rs34126013 |
Varsome | rs34126013 |
LitVar | rs34126013 |
Map | rs34126013 |
PheGenI | rs34126013 |
Biobank | rs34126013 |
1000 genomes | rs34126013 |
hgdp | rs34126013 |
ensembl | rs34126013 |
geneview | rs34126013 |
scholar | rs34126013 |
rs34126013 | |
pharmgkb | rs34126013 |
gwascentral | rs34126013 |
openSNP | rs34126013 |
23andMe | rs34126013 |
SNPshot | rs34126013 |
SNPdbe | rs34126013 |
MSV3d | rs34126013 |
GWAS Ctlg | rs34126013 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs34126013(T;T) |
Alt | rs34126013(T;T) |
Reference | Rs34126013(C;C) |
Significance | Pathogenic |
Disease | Hereditary cancer-predisposing syndrome not provided MYH-associated polyposis |
Variation | info |
Gene | MUTYH |
CLNDBN | Hereditary cancer-predisposing syndrome not provided MYH-associated polyposis |
Reversed | 1 |
HGVS | NC_000001.10:g.45798130G>A |
CLNSRC | |
CLNACC | RCV000164664.3, RCV000235834.1, RCV000369240.1, |