Gene: NR0B1 ×
Source: CLINVAR ×
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs104894897
rs104894897
NR0B1
C 0.810 CausalMutation CLINVAR

dbSNP: rs28935481
rs28935481
NR0B1
A 0.810 CausalMutation CLINVAR

dbSNP: rs104894888
rs104894888
NR0B1
G 0.800 CausalMutation CLINVAR

dbSNP: rs104894896
rs104894896
NR0B1
A 0.800 CausalMutation CLINVAR

dbSNP: rs104894899
rs104894899
NR0B1
T 0.800 CausalMutation CLINVAR

dbSNP: rs104894900
rs104894900
NR0B1
C 0.800 CausalMutation CLINVAR

dbSNP: rs104894907
rs104894907
NR0B1
G 0.800 CausalMutation CLINVAR

dbSNP: rs28935482
rs28935482
NR0B1
G 0.800 CausalMutation CLINVAR

dbSNP: rs387907373
rs387907373
NR0B1
A 0.710 CausalMutation CLINVAR

dbSNP: rs104894886
rs104894886
NR0B1
T 0.700 CausalMutation CLINVAR

dbSNP: rs104894887
rs104894887
NR0B1
T 0.700 CausalMutation CLINVAR

dbSNP: rs104894889
rs104894889
NR0B1
T 0.700 CausalMutation CLINVAR

dbSNP: rs104894890
rs104894890
NR0B1
A 0.700 CausalMutation CLINVAR

dbSNP: rs104894891
rs104894891
NR0B1
T 0.700 CausalMutation CLINVAR

dbSNP: rs104894892
rs104894892
NR0B1
T 0.700 CausalMutation CLINVAR

dbSNP: rs104894894
rs104894894
NR0B1
A 0.700 CausalMutation CLINVAR

dbSNP: rs104894895
rs104894895
NR0B1
C 0.700 CausalMutation CLINVAR

dbSNP: rs104894898
rs104894898
NR0B1
T 0.700 CausalMutation CLINVAR

dbSNP: rs104894906
rs104894906
NR0B1
T 0.700 CausalMutation CLINVAR

dbSNP: rs104894908
rs104894908
NR0B1
A 0.700 CausalMutation CLINVAR

dbSNP: rs1060499835
rs1060499835
NR0B1
G 0.700 GeneticVariation CLINVAR

dbSNP: rs1131691564
rs1131691564
NR0B1
T 0.700 CausalMutation CLINVAR

dbSNP: rs1311271225
rs1311271225
NR0B1
T 0.700 CausalMutation CLINVAR

dbSNP: rs1324519932
rs1324519932
NR0B1
A 0.700 CausalMutation CLINVAR

dbSNP: rs132630327
rs132630327
NR0B1
T 0.700 CausalMutation CLINVAR