Gene: TRIM37 ×
Source: CLINVAR ×
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs386834009
rs386834009
TRIM37
A 0.810 GeneticVariation CLINVAR

dbSNP: rs121908391
rs121908391
TRIM37
G 0.800 CausalMutation CLINVAR

dbSNP: rs386834004
rs386834004
TRIM37
G 0.800 GeneticVariation CLINVAR

dbSNP: rs373520509
rs373520509
TRIM37
A 0.700 CausalMutation CLINVAR

dbSNP: rs386833416
rs386833416
TRIM37
T 0.700 CausalMutation CLINVAR

dbSNP: rs386833999
rs386833999
TRIM37
CATCT 0.700 GeneticVariation CLINVAR

dbSNP: rs386834000
rs386834000
TRIM37
CT 0.700 GeneticVariation CLINVAR

dbSNP: rs386834001
rs386834001
TRIM37
A 0.700 GeneticVariation CLINVAR

dbSNP: rs386834002
rs386834002
TRIM37
T 0.700 GeneticVariation CLINVAR

dbSNP: rs386834003
rs386834003
TRIM37
A 0.700 GeneticVariation CLINVAR

dbSNP: rs386834006
rs386834006
TRIM37
T 0.700 GeneticVariation CLINVAR

dbSNP: rs386834007
rs386834007
TRIM37
A 0.700 GeneticVariation CLINVAR

dbSNP: rs386834008
rs386834008
TRIM37
T 0.700 CausalMutation CLINVAR

dbSNP: rs386834008
rs386834008
TRIM37
T 0.700 GeneticVariation CLINVAR