rs587776836
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs587776836(-;-) |
Make rs587776836(-;C) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 4 |
Position | 1801945 |
Gene | FGFR3 |
is a | snp |
is | mentioned by |
dbSNP | rs587776836 |
dbSNP (classic) | rs587776836 |
ClinGen | rs587776836 |
ebi | rs587776836 |
HLI | rs587776836 |
Exac | rs587776836 |
Gnomad | rs587776836 |
Varsome | rs587776836 |
LitVar | rs587776836 |
Map | rs587776836 |
PheGenI | rs587776836 |
Biobank | rs587776836 |
1000 genomes | rs587776836 |
hgdp | rs587776836 |
ensembl | rs587776836 |
geneview | rs587776836 |
scholar | rs587776836 |
rs587776836 | |
pharmgkb | rs587776836 |
gwascentral | rs587776836 |
openSNP | rs587776836 |
23andMe | rs587776836 |
SNPshot | rs587776836 |
SNPdbe | rs587776836 |
MSV3d | rs587776836 |
GWAS Ctlg | rs587776836 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs587776836(-;-) |
Alt | rs587776836(-;-) |
Reference | Rs587776836(C;C) |
Significance | Pathogenic |
Disease | Carcinoma of colon |
Variation | info |
Gene | FGFR3 |
CLNDBN | Carcinoma of colon |
Reversed | 0 |
HGVS | NC_000004.11:g.1803672delC |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000017762.5, |