rs876658941
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs876658941(G;T) |
Make rs876658941(T;T) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 5 |
Position | 112766410 |
Gene | APC |
is a | snp |
is | mentioned by |
dbSNP | rs876658941 |
dbSNP (classic) | rs876658941 |
ClinGen | rs876658941 |
ebi | rs876658941 |
HLI | rs876658941 |
Exac | rs876658941 |
Gnomad | rs876658941 |
Varsome | rs876658941 |
LitVar | rs876658941 |
Map | rs876658941 |
PheGenI | rs876658941 |
Biobank | rs876658941 |
1000 genomes | rs876658941 |
hgdp | rs876658941 |
ensembl | rs876658941 |
geneview | rs876658941 |
scholar | rs876658941 |
rs876658941 | |
pharmgkb | rs876658941 |
gwascentral | rs876658941 |
openSNP | rs876658941 |
23andMe | rs876658941 |
SNPshot | rs876658941 |
SNPdbe | rs876658941 |
MSV3d | rs876658941 |
GWAS Ctlg | rs876658941 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs876658941(T;T) |
Alt | rs876658941(T;T) |
Reference | Rs876658941(G;G) |
Significance | Pathogenic |
Disease | Hereditary cancer-predisposing syndrome not provided Familial adenomatous polyposis 1 |
Variation | info |
Gene | APC |
CLNDBN | Hereditary cancer-predisposing syndrome not provided Familial adenomatous polyposis 1 |
Reversed | 0 |
HGVS | NC_000005.9:g.112102107G>T |
CLNSRC | |
CLNACC | RCV000215333.1, RCV000254875.2, RCV000459175.1, |