Gene: ABCA12 ×
Source: CLINVAR ×
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1131692156
rs1131692156
ABCA12 ; SNHG31
C 0.700 GeneticVariation CLINVAR

dbSNP: rs11891778
rs11891778
ABCA12
A 0.700 CausalMutation CLINVAR

dbSNP: rs137853289
rs137853289
ABCA12 ; SNHG31
A 0.700 CausalMutation CLINVAR

dbSNP: rs1553520468
rs1553520468
ABCA12 ; SNHG31
G 0.700 GeneticVariation CLINVAR

dbSNP: rs1559120651
rs1559120651
ABCA12
AT 0.700 CausalMutation CLINVAR

dbSNP: rs1559134341
rs1559134341
ABCA12
G 0.700 GeneticVariation CLINVAR

dbSNP: rs199503269
rs199503269
ABCA12 ; SNHG31
A 0.700 CausalMutation CLINVAR

dbSNP: rs267606622
rs267606622
ABCA12
T 0.700 CausalMutation CLINVAR

dbSNP: rs28940269
rs28940269
ABCA12
C 0.700 GeneticVariation CLINVAR

dbSNP: rs387906284
rs387906284
ABCA12 ; SNHG31
C 0.700 CausalMutation CLINVAR

dbSNP: rs387906285
rs387906285
ABCA12
A 0.700 CausalMutation CLINVAR

dbSNP: rs761068277
rs761068277
ABCA12 ; SNHG31
T 0.700 GeneticVariation CLINVAR

dbSNP: rs764355087
rs764355087
ABCA12 ; SNHG31
A 0.700 GeneticVariation CLINVAR

dbSNP: rs771593783
rs771593783
ABCA12 ; SNHG31
A 0.700 GeneticVariation CLINVAR