rs387906236
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(-;AG) | 6.5 | Familial Adenomatous Polyposis |
(AG;AG) | 0 | common in clinvar |
Make rs387906236(-;-) |
Reference | GRCh38 38.1/141 |
Chromosome | 5 |
Position | 112840205 |
Gene | APC |
is a | snp |
is | mentioned by |
dbSNP | rs387906236 |
dbSNP (classic) | rs387906236 |
ClinGen | rs387906236 |
ebi | rs387906236 |
HLI | rs387906236 |
Exac | rs387906236 |
Gnomad | rs387906236 |
Varsome | rs387906236 |
LitVar | rs387906236 |
Map | rs387906236 |
PheGenI | rs387906236 |
Biobank | rs387906236 |
1000 genomes | rs387906236 |
hgdp | rs387906236 |
ensembl | rs387906236 |
geneview | rs387906236 |
scholar | rs387906236 |
rs387906236 | |
pharmgkb | rs387906236 |
gwascentral | rs387906236 |
openSNP | rs387906236 |
23andMe | rs387906236 |
SNPshot | rs387906236 |
SNPdbe | rs387906236 |
MSV3d | rs387906236 |
GWAS Ctlg | rs387906236 |
Max Magnitude | 6.5 |
ClinVar | |
---|---|
Risk | rs387906236(-;-) |
Alt | rs387906236(-;-) |
Reference | Rs387906236(AG;AG) |
Significance | Pathogenic |
Disease | Gardner syndrome |
Variation | info |
Gene | APC |
CLNDBN | Gardner syndrome |
Reversed | 0 |
HGVS | NC_000005.9:g.112175902_112175903delAG |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000000866.3, |