rs762307622
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs762307622(C;T) |
Make rs762307622(T;T) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 1 |
Position | 45332955 |
Gene | MUTYH |
is a | snp |
is | mentioned by |
dbSNP | rs762307622 |
dbSNP (classic) | rs762307622 |
ClinGen | rs762307622 |
ebi | rs762307622 |
HLI | rs762307622 |
Exac | rs762307622 |
Gnomad | rs762307622 |
Varsome | rs762307622 |
LitVar | rs762307622 |
Map | rs762307622 |
PheGenI | rs762307622 |
Biobank | rs762307622 |
1000 genomes | rs762307622 |
hgdp | rs762307622 |
ensembl | rs762307622 |
geneview | rs762307622 |
scholar | rs762307622 |
rs762307622 | |
pharmgkb | rs762307622 |
gwascentral | rs762307622 |
openSNP | rs762307622 |
23andMe | rs762307622 |
SNPshot | rs762307622 |
SNPdbe | rs762307622 |
MSV3d | rs762307622 |
GWAS Ctlg | rs762307622 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs762307622(T;T) |
Alt | rs762307622(T;T) |
Reference | Rs762307622(C;C) |
Significance | Other |
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.45798627C>T |
CLNSRC | |
CLNACC | RCV000213856.1, RCV000235993.1, RCV000411443.1, |