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rs3918018

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0
(G;G) 0 common in clinvar
Make rs3918018(A;A)
Make rs3918018(A;G)
ReferenceGRCh38 38.1/142
Chromosome1
Position36472277
GeneCSF3R
is asnp
is mentioned by
dbSNPrs3918018
dbSNP (old)rs3918018
ClinGenrs3918018
ebirs3918018
HLIrs3918018
Exacrs3918018
Gnomadrs3918018
Varsomers3918018
Maprs3918018
PheGenIrs3918018
Biobankrs3918018
1000 genomesrs3918018
hgdprs3918018
ensemblrs3918018
gopubmedrs3918018
geneviewrs3918018
scholarrs3918018
googlers3918018
pharmgkbrs3918018
gwascentralrs3918018
openSNPrs3918018
23andMers3918018
23andMe allrs3918018
SNP Nexus

SNPshotrs3918018
SNPdbers3918018
MSV3drs3918018
GWAS Ctlgrs3918018
GMAF0.01469
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 rs3918018(A;A)
Alt rs3918018(A;A)
Reference Rs3918018(G;G)
Significance Non-pathogenic
Disease not specified
Variation info
Gene CSF3R
CLNDBN not specified
Reversed 1
HGVS NC_000001.10:g.36937878C>T
CLNSRC
CLNACC RCV000249952.1,