rs374950566
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs374950566(A;A) |
Make rs374950566(A;G) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 1 |
Position | 45332215 |
Gene | MUTYH |
is a | snp |
is | mentioned by |
dbSNP | rs374950566 |
dbSNP (classic) | rs374950566 |
ClinGen | rs374950566 |
ebi | rs374950566 |
HLI | rs374950566 |
Exac | rs374950566 |
Gnomad | rs374950566 |
Varsome | rs374950566 |
LitVar | rs374950566 |
Map | rs374950566 |
PheGenI | rs374950566 |
Biobank | rs374950566 |
1000 genomes | rs374950566 |
hgdp | rs374950566 |
ensembl | rs374950566 |
geneview | rs374950566 |
scholar | rs374950566 |
rs374950566 | |
pharmgkb | rs374950566 |
gwascentral | rs374950566 |
openSNP | rs374950566 |
23andMe | rs374950566 |
SNPshot | rs374950566 |
SNPdbe | rs374950566 |
MSV3d | rs374950566 |
GWAS Ctlg | rs374950566 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs374950566(A;A) |
Alt | rs374950566(A;A) |
Reference | Rs374950566(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.45797887G>A |
CLNSRC | |
CLNACC | RCV000164625.2, RCV000235921.1, RCV000456980.1, |