rs140342925
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs140342925(C;T) |
Make rs140342925(T;T) |
Reference | GRCh38 38.1/142 |
Chromosome | 1 |
Position | 45332445 |
Gene | MUTYH |
is a | snp |
is | mentioned by |
dbSNP | rs140342925 |
dbSNP (classic) | rs140342925 |
ClinGen | rs140342925 |
ebi | rs140342925 |
HLI | rs140342925 |
Exac | rs140342925 |
Gnomad | rs140342925 |
Varsome | rs140342925 |
LitVar | rs140342925 |
Map | rs140342925 |
PheGenI | rs140342925 |
Biobank | rs140342925 |
1000 genomes | rs140342925 |
hgdp | rs140342925 |
ensembl | rs140342925 |
geneview | rs140342925 |
scholar | rs140342925 |
rs140342925 | |
pharmgkb | rs140342925 |
gwascentral | rs140342925 |
openSNP | rs140342925 |
23andMe | rs140342925 |
SNPshot | rs140342925 |
SNPdbe | rs140342925 |
MSV3d | rs140342925 |
GWAS Ctlg | rs140342925 |
Max Magnitude | 0 |
aka c.734G>A (p.Arg245His)
ClinVar | |
---|---|
Risk | rs140342925(T;T) |
Alt | rs140342925(T;T) |
Reference | Rs140342925(C;C) |
Significance | Other |
Disease | Hereditary cancer-predisposing syndrome MYH-associated polyposis not provided |
Variation | info |
Gene | MUTYH |
CLNDBN | Hereditary cancer-predisposing syndrome MYH-associated polyposis not provided |
Reversed | 0 |
HGVS | NC_000001.10:g.45798117C>T |
CLNSRC | Ambry Genetics ClinVar |
CLNACC | RCV000129105.7, RCV000196778.3, RCV000212706.2, |