Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs28937888
rs28937888
SLURP1
0.820 GeneticVariation BEFREE Patients with MDM with the homozygous SLURP-1 G86R mutation may have an impaired T-cell activation. 20854438

2011
dbSNP: rs28937888
rs28937888
SLURP1
0.820 GeneticVariation BEFREE Transfected human embryonic kidney 293T cells expressed the MDM mutant SLURP1 containing the single amino-acid substitution G86R but did not tolerate the MDM mutation W15R located in the signal peptide. 17008884

2007
dbSNP: rs28937888
rs28937888
SLURP1
G 0.820 CausalMutation CLINVAR

dbSNP: rs28937888
rs28937888
SLURP1
0.820 GeneticVariation UNIPROT

dbSNP: rs28937888
rs28937888
SLURP1
T 0.820 CausalMutation CLINVAR