rs730881833
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs730881833(A;A) |
Make rs730881833(A;G) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 1 |
Position | 45332242 |
Gene | MUTYH |
is a | snp |
is | mentioned by |
dbSNP | rs730881833 |
dbSNP (classic) | rs730881833 |
ClinGen | rs730881833 |
ebi | rs730881833 |
HLI | rs730881833 |
Exac | rs730881833 |
Gnomad | rs730881833 |
Varsome | rs730881833 |
LitVar | rs730881833 |
Map | rs730881833 |
PheGenI | rs730881833 |
Biobank | rs730881833 |
1000 genomes | rs730881833 |
hgdp | rs730881833 |
ensembl | rs730881833 |
geneview | rs730881833 |
scholar | rs730881833 |
rs730881833 | |
pharmgkb | rs730881833 |
gwascentral | rs730881833 |
openSNP | rs730881833 |
23andMe | rs730881833 |
SNPshot | rs730881833 |
SNPdbe | rs730881833 |
MSV3d | rs730881833 |
GWAS Ctlg | rs730881833 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs730881833(A;A) rs730881833(T;T) |
Alt | rs730881833(A;A) rs730881833(T;T) |
Reference | Rs730881833(G;G) |
Significance | Other |
Disease | not provided MYH-associated polyposis Hereditary cancer-predisposing syndrome |
Variation | info |
Gene | MUTYH |
CLNDBN | not provided MYH-associated polyposis Hereditary cancer-predisposing syndrome |
Reversed | 1 |
HGVS | NC_000001.10:g.45797914C>T |
CLNSRC | |
CLNACC | RCV000160754.2, RCV000191933.1, RCV000221854.2, |