rs137854570
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs137854570(C;G) |
Make rs137854570(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 5 |
Position | 112837732 |
Gene | APC |
is a | snp |
is | mentioned by |
dbSNP | rs137854570 |
dbSNP (classic) | rs137854570 |
ClinGen | rs137854570 |
ebi | rs137854570 |
HLI | rs137854570 |
Exac | rs137854570 |
Gnomad | rs137854570 |
Varsome | rs137854570 |
LitVar | rs137854570 |
Map | rs137854570 |
PheGenI | rs137854570 |
Biobank | rs137854570 |
1000 genomes | rs137854570 |
hgdp | rs137854570 |
ensembl | rs137854570 |
geneview | rs137854570 |
scholar | rs137854570 |
rs137854570 | |
pharmgkb | rs137854570 |
gwascentral | rs137854570 |
openSNP | rs137854570 |
23andMe | rs137854570 |
SNPshot | rs137854570 |
SNPdbe | rs137854570 |
MSV3d | rs137854570 |
GWAS Ctlg | rs137854570 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs137854570(G;G) |
Alt | rs137854570(G;G) |
Reference | Rs137854570(C;C) |
Significance | Pathogenic |
Disease | Gardner syndrome Hereditary cancer-predisposing syndrome |
Variation | info |
Gene | APC |
CLNDBN | Gardner syndrome Hereditary cancer-predisposing syndrome |
Reversed | 0 |
HGVS | NC_000005.9:g.112173429C>G |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000000837.5, RCV000491636.1, |