Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1423415130
rs1423415130
XYLT2
A 0.700 GeneticVariation CLINVAR

dbSNP: rs797044806
rs797044806
XYLT2
GC 0.700 CausalMutation CLINVAR

dbSNP: rs797044807
rs797044807
XYLT2
T 0.700 CausalMutation CLINVAR

dbSNP: rs4364254
rs4364254
HPSE
0.010 GeneticVariation BEFREE In addition, incidence of SOS in patients with genotype CC or CT of rs4364254 (C>T) was significantly decreased in comparison with patients with genotype TT (2.3 vs. 14.7 %, P = 0.004). 25335953

2015
dbSNP: rs4693608
rs4693608
HPSE
0.010 GeneticVariation BEFREE Patients with HPSE genotypes GG or AG of rs4693608 (G>A) had a significantly reduced incidence of SOS on day 100 after HSCT compared to patients with genotype AA (4.7 vs. 14.3 %, P = 0.038). 25335953

2015