SERPINB6, serpin family B member 6, 5269

N. diseases: 128; N. variants: 3
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs73718779
rs73718779
Entrez Id: 5269
Gene Symbol: SERPINB6
SERPINB6
CUI: C0855095
Disease:
Small Lymphocytic Lymphoma 		A 0.700 GeneticVariation GWASCAT Meta-analysis of genome-wide association studies discovers multiple loci for chronic lymphocytic leukemia. 26956414 2016
dbSNP: rs73718779
rs73718779
Entrez Id: 5269
Gene Symbol: SERPINB6
SERPINB6
CUI: C0023434
Disease:
Chronic Lymphocytic Leukemia 		A 0.700 GeneticVariation GWASCAT Meta-analysis of genome-wide association studies discovers multiple loci for chronic lymphocytic leukemia. 26956414 2016
dbSNP: rs267607037
rs267607037
Entrez Id: 5269
Gene Symbol: SERPINB6
SERPINB6
CUI: C3150704
Disease:
DEAFNESS, AUTOSOMAL RECESSIVE 91 		A 0.700 CausalMutation CLINVAR
dbSNP: rs1325863623
rs1325863623
Entrez Id: 5269
Gene Symbol: SERPINB6
SERPINB6
CUI: C0023895
Disease:
Liver diseases 		0.010 GeneticVariation BEFREE The PNPLA3 p.I148M, TM6SF2 p.E167K and MBOAT7 p.G17E variants represent genetic determinants for progressive liver diseases. 31669075 2020