rs121913329
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs121913329(C;T) |
Make rs121913329(T;T) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 5 |
Position | 112839726 |
Gene | APC |
is a | snp |
is | mentioned by |
dbSNP | rs121913329 |
dbSNP (classic) | rs121913329 |
ClinGen | rs121913329 |
ebi | rs121913329 |
HLI | rs121913329 |
Exac | rs121913329 |
Gnomad | rs121913329 |
Varsome | rs121913329 |
LitVar | rs121913329 |
Map | rs121913329 |
PheGenI | rs121913329 |
Biobank | rs121913329 |
1000 genomes | rs121913329 |
hgdp | rs121913329 |
ensembl | rs121913329 |
geneview | rs121913329 |
scholar | rs121913329 |
rs121913329 | |
pharmgkb | rs121913329 |
gwascentral | rs121913329 |
openSNP | rs121913329 |
23andMe | rs121913329 |
SNPshot | rs121913329 |
SNPdbe | rs121913329 |
MSV3d | rs121913329 |
GWAS Ctlg | rs121913329 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs121913329(T;T) |
Alt | rs121913329(T;T) |
Reference | Rs121913329(C;C) |
Significance | Probable-Pathogenic |
Disease | Colorectal Neoplasms |
Variation | info |
Gene | APC |
CLNDBN | Colorectal Neoplasms |
Reversed | 0 |
HGVS | NC_000005.9:g.112175423C>T |
CLNSRC | |
CLNACC | RCV000443420.1, |