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rs1801117

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1801117(C;T)
Make rs1801117(T;T)
ReferenceGRCh38 38.1/141
Chromosome22
Position36933957
GeneCSF2RB
is asnp
is mentioned by
dbSNPrs1801117
ebirs1801117
HLIrs1801117
Exacrs1801117
Varsomers1801117
Maprs1801117
PheGenIrs1801117
hapmaprs1801117
1000 genomesrs1801117
hgdprs1801117
ensemblrs1801117
gopubmedrs1801117
geneviewrs1801117
scholarrs1801117
googlers1801117
pharmgkbrs1801117
gwascentralrs1801117
openSNPrs1801117
23andMers1801117
23andMe allrs1801117
SNP Nexus

SNPshotrs1801117
SNPdbers1801117
MSV3drs1801117
GWAS Ctlgrs1801117
Merged fromRs7285064
GMAF0.1648
Max Magnitude0
[PMID 17667962OA-icon.png] Association study of CSF2RB with schizophrenia in Irish family and case - control samples.

[PMID 18804346OA-icon.png] Interaction between interleukin 3 and dystrobrevin-binding protein 1 in schizophrenia.

ClinVar
Risk rs1801117(T;T)
Alt rs1801117(T;T)
Reference rs1801117(C;C)
Significance Non-pathogenic
Disease not specified
Variation info
Gene CSF2RB
CLNDBN not specified
Reversed 0
HGVS NC_000022.10:g.37329999C>T
CLNSRC
CLNACC RCV000216776.1,