SIRPB1, signal regulatory protein beta 1, 10326

N. diseases: 10; N. variants: 7
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2243602
rs2243602
Entrez Id: 10326
Gene Symbol: SIRPB1
SIRPB1
CUI: C0023508
Disease:
White Blood Cell Count procedure
0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs12480824
rs12480824
Entrez Id: 10326
Gene Symbol: SIRPB1
SIRPB1
CUI: C2985280
Disease:
Blood Protein Measurement
T 0.700 GeneticVariation GWASCAT Genomic atlas of the human plasma proteome. 29875488 2018
dbSNP: rs2244133
rs2244133
Entrez Id: 10326
Gene Symbol: SIRPB1
SIRPB1
CUI: C2985280
Disease:
Blood Protein Measurement
T 0.700 GeneticVariation GWASCAT Genomic atlas of the human plasma proteome. 29875488 2018
dbSNP: rs41275422
rs41275422
Entrez Id: 10326
Gene Symbol: SIRPB1
SIRPB1
CUI: C2985280
Disease:
Blood Protein Measurement
G 0.700 GeneticVariation GWASCAT Genomic atlas of the human plasma proteome. 29875488 2018
dbSNP: rs76357893
rs76357893
Entrez Id: 10326
Gene Symbol: SIRPB1
SIRPB1
CUI: C2985280
Disease:
Blood Protein Measurement
G 0.700 GeneticVariation GWASCAT Genomic atlas of the human plasma proteome. 29875488 2018
dbSNP: rs11696739
rs11696739
Entrez Id: 10326
Gene Symbol: SIRPB1
SIRPB1
CUI: C0200665
Disease:
Platelet mean volume determination (procedure)
A 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs2209313
rs2209313
Entrez Id: 10326
Gene Symbol: SIRPB1
SIRPB1
CUI: C0600139
Disease:
Prostate carcinoma
0.010 GeneticVariation BEFREE Pooled analysis using all 3353 aggressive and 3584 nonaggressive cases showed the T allele of rs2209313 was significantly associated with an increased risk of aggressive PCa (OR = 1.17, 95% CI: 1.07-1.27; P = 2.75 × 10(-4)). 21551127 2011
dbSNP: rs2209313
rs2209313
Entrez Id: 10326
Gene Symbol: SIRPB1
SIRPB1
CUI: C0376358
Disease:
Malignant neoplasm of prostate
0.010 GeneticVariation BEFREE Pooled analysis using all 3353 aggressive and 3584 nonaggressive cases showed the T allele of rs2209313 was significantly associated with an increased risk of aggressive PCa (OR = 1.17, 95% CI: 1.07-1.27; P = 2.75 × 10(-4)). 21551127 2011