Gene: CASP8 ×
Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1045485
rs1045485
CASP8
0.010 GeneticVariation BEFREE The primary aim of this study was, therefore, to investigate previously implicated DNA sequence variants within CASP8: rs3834129 (ins/del) and rs1045485 (G/C), and the rs13113 (T/A) identified using a whole exome sequencing approach, with risk of musculoskeletal injury phenotypes (RCT, ACL ruptures, and CTS) in three independent studies. 31692049

2020
dbSNP: rs13113
rs13113
CASP8
0.010 GeneticVariation BEFREE It was found that the AA genotype of CASP8 rs13113 (T/A) was independently associated with increased risk for CTS. 31692049

2020
dbSNP: rs3834129
rs3834129
CASP8
0.010 GeneticVariation BEFREE The primary aim of this study was, therefore, to investigate previously implicated DNA sequence variants within CASP8: rs3834129 (ins/del) and rs1045485 (G/C), and the rs13113 (T/A) identified using a whole exome sequencing approach, with risk of musculoskeletal injury phenotypes (RCT, ACL ruptures, and CTS) in three independent studies. 31692049

2020