rs3918001
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | |
(G;G) | 0 | common in clinvar |
Make rs3918001(A;A) |
Make rs3918001(A;G) |
Reference | GRCh38 38.1/142 |
Chromosome | 1 |
Position | 36466902 |
Gene | CSF3R |
is a | snp |
is | mentioned by |
dbSNP | rs3918001 |
dbSNP (classic) | rs3918001 |
ClinGen | rs3918001 |
ebi | rs3918001 |
HLI | rs3918001 |
Exac | rs3918001 |
Gnomad | rs3918001 |
Varsome | rs3918001 |
LitVar | rs3918001 |
Map | rs3918001 |
PheGenI | rs3918001 |
Biobank | rs3918001 |
1000 genomes | rs3918001 |
hgdp | rs3918001 |
ensembl | rs3918001 |
geneview | rs3918001 |
scholar | rs3918001 |
rs3918001 | |
pharmgkb | rs3918001 |
gwascentral | rs3918001 |
openSNP | rs3918001 |
23andMe | rs3918001 |
SNPshot | rs3918001 |
SNPdbe | rs3918001 |
MSV3d | rs3918001 |
GWAS Ctlg | rs3918001 |
GMAF | 0.04178 |
Max Magnitude | 0 |
? | (A;A) (A;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 | rs3918001(A;A) |
Alt | rs3918001(A;A) |
Reference | Rs3918001(G;G) |
Significance | Non-pathogenic |
Disease | not specified |
Variation | info |
Gene | CSF3R |
CLNDBN | not specified |
Reversed | 1 |
HGVS | NC_000001.10:g.36932503C>T |
CLNSRC | |
CLNACC | RCV000242925.1, |