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rs3918001

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0
(G;G) 0 common in clinvar
Make rs3918001(A;A)
Make rs3918001(A;G)
ReferenceGRCh38 38.1/142
Chromosome1
Position36466902
GeneCSF3R
is asnp
is mentioned by
dbSNPrs3918001
dbSNP (classic)rs3918001
ClinGenrs3918001
ebirs3918001
HLIrs3918001
Exacrs3918001
Gnomadrs3918001
Varsomers3918001
LitVarrs3918001
Maprs3918001
PheGenIrs3918001
Biobankrs3918001
1000 genomesrs3918001
hgdprs3918001
ensemblrs3918001
geneviewrs3918001
scholarrs3918001
googlers3918001
pharmgkbrs3918001
gwascentralrs3918001
openSNPrs3918001
23andMers3918001
SNPshotrs3918001
SNPdbers3918001
MSV3drs3918001
GWAS Ctlgrs3918001
GMAF0.04178
Max Magnitude0
? (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,