rs121913393
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Make rs121913393(C;C) |
Make rs121913393(C;T) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 5 |
Position | 150054083 |
Gene | CSF1R |
is a | snp |
is | mentioned by |
dbSNP | rs121913393 |
dbSNP (classic) | rs121913393 |
ClinGen | rs121913393 |
ebi | rs121913393 |
HLI | rs121913393 |
Exac | rs121913393 |
Gnomad | rs121913393 |
Varsome | rs121913393 |
LitVar | rs121913393 |
Map | rs121913393 |
PheGenI | rs121913393 |
Biobank | rs121913393 |
1000 genomes | rs121913393 |
hgdp | rs121913393 |
ensembl | rs121913393 |
geneview | rs121913393 |
scholar | rs121913393 |
rs121913393 | |
pharmgkb | rs121913393 |
gwascentral | rs121913393 |
openSNP | rs121913393 |
23andMe | rs121913393 |
SNPshot | rs121913393 |
SNPdbe | rs121913393 |
MSV3d | rs121913393 |
GWAS Ctlg | rs121913393 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs121913393(C;C) |
Alt | rs121913393(C;C) |
Reference | Rs121913393(T;T) |
Significance | Probable-Pathogenic |
Disease | Neoplasm Hematologic neoplasm |
Variation | info |
Gene | CSF1R |
CLNDBN | Neoplasm Hematologic neoplasm |
Reversed | 1 |
HGVS | NC_000005.9:g.149433646A>G |
CLNSRC | |
CLNACC | RCV000423228.1, RCV000434345.1, |