rs3917991
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs3917991(C;C) |
Make rs3917991(C;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 1 |
Position | 36469204 |
Gene | CSF3R |
is a | snp |
is | mentioned by |
dbSNP | rs3917991 |
dbSNP (classic) | rs3917991 |
ClinGen | rs3917991 |
ebi | rs3917991 |
HLI | rs3917991 |
Exac | rs3917991 |
Gnomad | rs3917991 |
Varsome | rs3917991 |
LitVar | rs3917991 |
Map | rs3917991 |
PheGenI | rs3917991 |
Biobank | rs3917991 |
1000 genomes | rs3917991 |
hgdp | rs3917991 |
ensembl | rs3917991 |
geneview | rs3917991 |
scholar | rs3917991 |
rs3917991 | |
pharmgkb | rs3917991 |
gwascentral | rs3917991 |
openSNP | rs3917991 |
23andMe | rs3917991 |
SNPshot | rs3917991 |
SNPdbe | rs3917991 |
MSV3d | rs3917991 |
GWAS Ctlg | rs3917991 |
GMAF | 0.05051 |
Max Magnitude | 0 |
? | (C;C) (C;G) (G;G) | 28 |
---|---|---|
|
[PMID 23159284] The effect of granulocyte colony stimulating factor receptor gene missense single nucleotide polymorphisms on peripheral blood stem cell enrichment
ClinVar | |
---|---|
Risk | rs3917991(A;A) rs3917991(C;C) |
Alt | rs3917991(A;A) rs3917991(C;C) |
Reference | Rs3917991(G;G) |
Significance | Non-pathogenic |
Disease | not specified |
Variation | info |
Gene | CSF3R |
CLNDBN | not specified |
Reversed | 1 |
HGVS | NC_000001.10:g.36934805C>G |
CLNSRC | |
CLNACC | RCV000245449.1, |