rs138775799
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs138775799(A;A) |
Make rs138775799(A;G) |
Reference | GRCh38 38.1/142 |
Chromosome | 1 |
Position | 45333472 |
Gene | MUTYH |
is a | snp |
is | mentioned by |
dbSNP | rs138775799 |
dbSNP (classic) | rs138775799 |
ClinGen | rs138775799 |
ebi | rs138775799 |
HLI | rs138775799 |
Exac | rs138775799 |
Gnomad | rs138775799 |
Varsome | rs138775799 |
LitVar | rs138775799 |
Map | rs138775799 |
PheGenI | rs138775799 |
Biobank | rs138775799 |
1000 genomes | rs138775799 |
hgdp | rs138775799 |
ensembl | rs138775799 |
geneview | rs138775799 |
scholar | rs138775799 |
rs138775799 | |
pharmgkb | rs138775799 |
gwascentral | rs138775799 |
openSNP | rs138775799 |
23andMe | rs138775799 |
SNPshot | rs138775799 |
SNPdbe | rs138775799 |
MSV3d | rs138775799 |
GWAS Ctlg | rs138775799 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs138775799(A;A) |
Alt | rs138775799(A;A) |
Reference | Rs138775799(G;G) |
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 | 0 |
HGVS | NC_000001.10:g.45799144G>A |
CLNSRC | Ambry Genetics ClinVar |
CLNACC | RCV000129018.3, RCV000235267.1, RCV000471769.1, |