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rs3917991

From SNPedia

Orientationminus
Stabilizedminus
Make rs3917991(C;C)
Make rs3917991(C;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position36469204
GeneCSF3R
is asnp
is mentioned by
dbSNPrs3917991
dbSNP (classic)rs3917991
ClinGenrs3917991
ebirs3917991
HLIrs3917991
Exacrs3917991
Gnomadrs3917991
Varsomers3917991
LitVarrs3917991
Maprs3917991
PheGenIrs3917991
Biobankrs3917991
1000 genomesrs3917991
hgdprs3917991
ensemblrs3917991
geneviewrs3917991
scholarrs3917991
googlers3917991
pharmgkbrs3917991
gwascentralrs3917991
openSNPrs3917991
23andMers3917991
SNPshotrs3917991
SNPdbers3917991
MSV3drs3917991
GWAS Ctlgrs3917991
GMAF0.05051
Max Magnitude0
? (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,