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rs121918426

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121918426(A;A)
Make rs121918426(A;C)
ReferenceGRCh38 38.1/141
Chromosome1
Position36467597
GeneCSF3R
is asnp
is mentioned by
dbSNPrs121918426
ebirs121918426
HLIrs121918426
Exacrs121918426
Varsomers121918426
Maprs121918426
PheGenIrs121918426
hapmaprs121918426
1000 genomesrs121918426
hgdprs121918426
ensemblrs121918426
gopubmedrs121918426
geneviewrs121918426
scholarrs121918426
googlers121918426
pharmgkbrs121918426
gwascentralrs121918426
openSNPrs121918426
23andMers121918426
23andMe allrs121918426
SNP Nexus

SNPshotrs121918426
SNPdbers121918426
MSV3drs121918426
GWAS Ctlgrs121918426
GMAF0.0004591
Max Magnitude0
OMIM138971
Desc
Variant0001
Relatedalso
ClinVar
Risk rs121918426(A,T;A,T)
Alt rs121918426(A,T;A,T)
Reference rs121918426(C;C)
Significance Pathogenic
Disease Hereditary neutrophilia
Variation info
Gene CSF3R
CLNDBN Hereditary neutrophilia
Reversed 1
HGVS NC_000001.10:g.36933198G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000017378.29,