Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs80359845
rs80359845
G 0.700 CausalMutation CLINVAR The molecular mechanism underlying Roberts syndrome involves loss of ESCO2 acetyltransferase activity. 18411254

2008

dbSNP: rs146312522
rs146312522
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1554554098
rs1554554098
TG 0.700 CausalMutation CLINVAR

dbSNP: rs1554555716
rs1554555716
AG 0.700 CausalMutation CLINVAR

dbSNP: rs797045565
rs797045565
TTTTAT 0.700 CausalMutation CLINVAR

dbSNP: rs797045566
rs797045566
TA 0.700 CausalMutation CLINVAR

dbSNP: rs80359844
rs80359844
G 0.700 CausalMutation CLINVAR

dbSNP: rs80359846
rs80359846
T 0.700 CausalMutation CLINVAR

dbSNP: rs80359847
rs80359847
T 0.700 CausalMutation CLINVAR

dbSNP: rs80359848
rs80359848
CA 0.700 CausalMutation CLINVAR

dbSNP: rs80359849
rs80359849
T 0.700 CausalMutation CLINVAR

dbSNP: rs80359850
rs80359850
T 0.700 CausalMutation CLINVAR

dbSNP: rs80359851
rs80359851
C 0.700 CausalMutation CLINVAR

dbSNP: rs80359852
rs80359852
G 0.700 CausalMutation CLINVAR

dbSNP: rs80359852
rs80359852
GA 0.700 CausalMutation CLINVAR

dbSNP: rs80359855
rs80359855
C 0.700 CausalMutation CLINVAR

dbSNP: rs80359856
rs80359856
T 0.700 CausalMutation CLINVAR

dbSNP: rs80359857
rs80359857
C 0.700 CausalMutation CLINVAR

dbSNP: rs80359858
rs80359858
C 0.700 CausalMutation CLINVAR

dbSNP: rs80359859
rs80359859
TA 0.700 CausalMutation CLINVAR

dbSNP: rs80359859
rs80359859
TA 0.700 GeneticVariation CLINVAR

dbSNP: rs80359861
rs80359861
A 0.700 CausalMutation CLINVAR

dbSNP: rs80359862
rs80359862
G 0.700 CausalMutation CLINVAR

dbSNP: rs80359863
rs80359863
C 0.700 CausalMutation CLINVAR

dbSNP: rs80359864
rs80359864
A 0.700 CausalMutation CLINVAR