rs121913472
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs121913472(A;A) |
Make rs121913472(A;C) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 8 |
Position | 38424691 |
Gene | FGFR1 |
is a | snp |
is | mentioned by |
dbSNP | rs121913472 |
dbSNP (classic) | rs121913472 |
ClinGen | rs121913472 |
ebi | rs121913472 |
HLI | rs121913472 |
Exac | rs121913472 |
Gnomad | rs121913472 |
Varsome | rs121913472 |
LitVar | rs121913472 |
Map | rs121913472 |
PheGenI | rs121913472 |
Biobank | rs121913472 |
1000 genomes | rs121913472 |
hgdp | rs121913472 |
ensembl | rs121913472 |
geneview | rs121913472 |
scholar | rs121913472 |
rs121913472 | |
pharmgkb | rs121913472 |
gwascentral | rs121913472 |
openSNP | rs121913472 |
23andMe | rs121913472 |
SNPshot | rs121913472 |
SNPdbe | rs121913472 |
MSV3d | rs121913472 |
GWAS Ctlg | rs121913472 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs121913472(A;A) |
Alt | rs121913472(A;A) |
Reference | Rs121913472(C;C) |
Significance | Probable-Pathogenic |
Disease | Neoplasm |
Variation | info |
Gene | FGFR1 |
CLNDBN | Neoplasm |
Reversed | 1 |
HGVS | NC_000008.10:g.38282209G>T |
CLNSRC | |
CLNACC | RCV000436130.1, |