rs587780749
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs587780749(G;T) |
Make rs587780749(T;T) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 1 |
Position | 45332443 |
Gene | MUTYH |
is a | snp |
is | mentioned by |
dbSNP | rs587780749 |
dbSNP (classic) | rs587780749 |
ClinGen | rs587780749 |
ebi | rs587780749 |
HLI | rs587780749 |
Exac | rs587780749 |
Gnomad | rs587780749 |
Varsome | rs587780749 |
LitVar | rs587780749 |
Map | rs587780749 |
PheGenI | rs587780749 |
Biobank | rs587780749 |
1000 genomes | rs587780749 |
hgdp | rs587780749 |
ensembl | rs587780749 |
geneview | rs587780749 |
scholar | rs587780749 |
rs587780749 | |
pharmgkb | rs587780749 |
gwascentral | rs587780749 |
openSNP | rs587780749 |
23andMe | rs587780749 |
SNPshot | rs587780749 |
SNPdbe | rs587780749 |
MSV3d | rs587780749 |
GWAS Ctlg | rs587780749 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs587780749(A;A) rs587780749(T;T) |
Alt | rs587780749(A;A) rs587780749(T;T) |
Reference | Rs587780749(G;G) |
Significance | Other |
Disease | MYH-associated polyposis Hereditary cancer-predisposing syndrome not provided not specified |
Variation | info |
Gene | MUTYH |
CLNDBN | MYH-associated polyposis Hereditary cancer-predisposing syndrome not provided not specified |
Reversed | 1 |
HGVS | NC_000001.10:g.45798115C>A; NC_000001.10:g.45798115C>T |
CLNSRC | |
CLNACC | RCV000123154.2, RCV000131615.7, RCV000212707.2, RCV000222948.1, RCV000475824.1, RCV000485797.1, |