rs397514032
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in clinvar |
Make rs397514032(-;-) |
Make rs397514032(-;A) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 5 |
Position | 112828924 |
Gene | APC |
is a | snp |
is | mentioned by |
dbSNP | rs397514032 |
dbSNP (classic) | rs397514032 |
ClinGen | rs397514032 |
ebi | rs397514032 |
HLI | rs397514032 |
Exac | rs397514032 |
Gnomad | rs397514032 |
Varsome | rs397514032 |
LitVar | rs397514032 |
Map | rs397514032 |
PheGenI | rs397514032 |
Biobank | rs397514032 |
1000 genomes | rs397514032 |
hgdp | rs397514032 |
ensembl | rs397514032 |
geneview | rs397514032 |
scholar | rs397514032 |
rs397514032 | |
pharmgkb | rs397514032 |
gwascentral | rs397514032 |
openSNP | rs397514032 |
23andMe | rs397514032 |
SNPshot | rs397514032 |
SNPdbe | rs397514032 |
MSV3d | rs397514032 |
GWAS Ctlg | rs397514032 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs397514032(-;-) |
Alt | rs397514032(-;-) |
Reference | Rs397514032(A;A) |
Significance | Pathogenic |
Disease | Hepatocellular carcinoma |
Variation | info |
Gene | APC |
CLNDBN | Hepatocellular carcinoma |
Reversed | 0 |
HGVS | NC_000005.9:g.112164621delA |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000000883.5, |