Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1064796472
rs1064796472
SON
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1114167303
rs1114167303
SON
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1275312464
rs1275312464
SON
T 0.700 CausalMutation CLINVAR

dbSNP: rs1555898531
rs1555898531
SON
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1569050345
rs1569050345
G 0.700 GeneticVariation CLINVAR

dbSNP: rs1569053308
rs1569053308
C 0.700 GeneticVariation CLINVAR

dbSNP: rs1569055781
rs1569055781
SON
TGC 0.700 GeneticVariation CLINVAR

dbSNP: rs1569056484
rs1569056484
SON
G 0.700 GeneticVariation CLINVAR

dbSNP: rs1569057333
rs1569057333
SON
AG 0.700 GeneticVariation CLINVAR

dbSNP: rs1569058041
rs1569058041
SON
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1569059792
rs1569059792
SON
G 0.700 GeneticVariation CLINVAR

dbSNP: rs769691894
rs769691894
SON
A 0.700 GeneticVariation CLINVAR

dbSNP: rs778418096
rs778418096
G 0.700 CausalMutation CLINVAR

dbSNP: rs886039773
rs886039773
SON
C 0.700 CausalMutation CLINVAR

dbSNP: rs886039773
rs886039773
SON
C 0.700 GeneticVariation CLINVAR

dbSNP: rs886039774
rs886039774
SON
A 0.700 GeneticVariation CLINVAR

dbSNP: rs886039774
rs886039774
SON
A 0.700 CausalMutation CLINVAR

dbSNP: rs886039775
rs886039775
SON
TCC 0.700 CausalMutation CLINVAR

dbSNP: rs886039775
rs886039775
SON
TCC 0.700 GeneticVariation CLINVAR

dbSNP: rs886039776
rs886039776
SON
C 0.700 CausalMutation CLINVAR

dbSNP: rs886039776
rs886039776
SON
C 0.700 GeneticVariation CLINVAR

dbSNP: rs886039777
rs886039777
T 0.700 CausalMutation CLINVAR

dbSNP: rs886039778
rs886039778
SON
GA 0.700 CausalMutation CLINVAR

dbSNP: rs886039779
rs886039779
SON
A 0.700 CausalMutation CLINVAR