rs1060501342
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(-;CC) | 4 | increased risk for several cancers |
(CC;CC) | 0 | common in clinvar |
Make rs1060501342(-;-) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 1 |
Position | 45331746 |
Gene | MUTYH |
is a | snp |
is | mentioned by |
dbSNP | rs1060501342 |
dbSNP (classic) | rs1060501342 |
ClinGen | rs1060501342 |
ebi | rs1060501342 |
HLI | rs1060501342 |
Exac | rs1060501342 |
Gnomad | rs1060501342 |
Varsome | rs1060501342 |
LitVar | rs1060501342 |
Map | rs1060501342 |
PheGenI | rs1060501342 |
Biobank | rs1060501342 |
1000 genomes | rs1060501342 |
hgdp | rs1060501342 |
ensembl | rs1060501342 |
geneview | rs1060501342 |
scholar | rs1060501342 |
rs1060501342 | |
pharmgkb | rs1060501342 |
gwascentral | rs1060501342 |
openSNP | rs1060501342 |
23andMe | rs1060501342 |
SNPshot | rs1060501342 |
SNPdbe | rs1060501342 |
MSV3d | rs1060501342 |
GWAS Ctlg | rs1060501342 |
Max Magnitude | 4 |
aka c.1100_1101delCC (p.Pro367Glnfs)
ClinVar | |
---|---|
Risk | rs1060501342(-;-) |
Alt | rs1060501342(-;-) |
Reference | Rs1060501342(CC;CC) |
Significance | Probable-Pathogenic |
Disease | MYH-associated polyposis |
Variation | info |
Gene | MUTYH |
CLNDBN | MYH-associated polyposis |
Reversed | 1 |
HGVS | NC_000001.10:g.45797418_45797419delGG |
CLNSRC | |
CLNACC | RCV000474499.1, |