rs786202724
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;G) | 5.7 | Familial papillary renal cell carcinoma |
(G;G) | 0 | common in clinvar |
Make rs786202724(A;A) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 7 |
Position | 116777403 |
Gene | MET |
is a | snp |
is | mentioned by |
dbSNP | rs786202724 |
dbSNP (classic) | rs786202724 |
ClinGen | rs786202724 |
ebi | rs786202724 |
HLI | rs786202724 |
Exac | rs786202724 |
Gnomad | rs786202724 |
Varsome | rs786202724 |
LitVar | rs786202724 |
Map | rs786202724 |
PheGenI | rs786202724 |
Biobank | rs786202724 |
1000 genomes | rs786202724 |
hgdp | rs786202724 |
ensembl | rs786202724 |
geneview | rs786202724 |
scholar | rs786202724 |
rs786202724 | |
pharmgkb | rs786202724 |
gwascentral | rs786202724 |
openSNP | rs786202724 |
23andMe | rs786202724 |
SNPshot | rs786202724 |
SNPdbe | rs786202724 |
MSV3d | rs786202724 |
GWAS Ctlg | rs786202724 |
Max Magnitude | 5.7 |
ClinVar | |
---|---|
Risk | rs786202724(A;A) |
Alt | rs786202724(A;A) |
Reference | Rs786202724(G;G) |
Significance | Pathogenic |
Disease | Hereditary cancer-predisposing syndrome Neoplasm Carcinoma |
Variation | info |
Gene | MET |
CLNDBN | Hereditary cancer-predisposing syndrome Neoplasm Carcinoma |
Reversed | 0 |
HGVS | NC_000007.13:g.116417457G>A |
CLNSRC | |
CLNACC | RCV000165679.1, RCV000425188.1, RCV000443267.1, |