Gene: NR0B1 ×
Source: CLINVAR ×
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs28935481
rs28935481
NR0B1
A 0.810 CausalMutation CLINVAR

dbSNP: rs104894896
rs104894896
NR0B1
A 0.800 CausalMutation CLINVAR

dbSNP: rs387907373
rs387907373
NR0B1
A 0.710 CausalMutation CLINVAR

dbSNP: rs104894890
rs104894890
NR0B1
A 0.700 CausalMutation CLINVAR

dbSNP: rs104894894
rs104894894
NR0B1
A 0.700 CausalMutation CLINVAR

dbSNP: rs104894908
rs104894908
NR0B1
A 0.700 CausalMutation CLINVAR

dbSNP: rs1324519932
rs1324519932
NR0B1
A 0.700 CausalMutation CLINVAR

dbSNP: rs1555972655
rs1555972655
NR0B1
A 0.700 CausalMutation CLINVAR

dbSNP: rs1555972994
rs1555972994
NR0B1
A 0.700 CausalMutation CLINVAR

dbSNP: rs1555973010
rs1555973010
NR0B1
A 0.700 CausalMutation CLINVAR

dbSNP: rs1555973031
rs1555973031
NR0B1
A 0.700 CausalMutation CLINVAR

dbSNP: rs386134263
rs386134263
NR0B1
A 0.700 CausalMutation CLINVAR

dbSNP: rs386134263
rs386134263
NR0B1
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1555973117
rs1555973117
NR0B1
AC 0.700 CausalMutation CLINVAR

dbSNP: rs104894897
rs104894897
NR0B1
C 0.810 CausalMutation CLINVAR

dbSNP: rs104894900
rs104894900
NR0B1
C 0.800 CausalMutation CLINVAR

dbSNP: rs104894895
rs104894895
NR0B1
C 0.700 CausalMutation CLINVAR

dbSNP: rs1555972640
rs1555972640
NR0B1
C 0.700 CausalMutation CLINVAR

dbSNP: rs1555973115
rs1555973115
NR0B1
C 0.700 CausalMutation CLINVAR

dbSNP: rs1555973120
rs1555973120
NR0B1
C 0.700 CausalMutation CLINVAR

dbSNP: rs1569268070
rs1569268070
NR0B1
C 0.700 CausalMutation CLINVAR

dbSNP: rs1569268976
rs1569268976
NR0B1
C 0.700 CausalMutation CLINVAR

dbSNP: rs767828388
rs767828388
NR0B1
C 0.700 CausalMutation CLINVAR

dbSNP: rs1555972632
rs1555972632
NR0B1
CA 0.700 CausalMutation CLINVAR

dbSNP: rs1555973119
rs1555973119
NR0B1
CTGGG 0.700 CausalMutation CLINVAR