Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs138305578
rs138305578
C 0.800 GeneticVariation CLINVAR

dbSNP: rs1399429058
rs1399429058
T 0.800 GeneticVariation CLINVAR

dbSNP: rs757209071
rs757209071
T 0.800 GeneticVariation CLINVAR

dbSNP: rs768222183
rs768222183
T 0.800 GeneticVariation CLINVAR

dbSNP: rs768222183
rs768222183
T 0.800 CausalMutation CLINVAR

dbSNP: rs778985686
rs778985686
T 0.800 GeneticVariation CLINVAR

dbSNP: rs778985686
rs778985686
T 0.800 CausalMutation CLINVAR

dbSNP: rs148932047
rs148932047
A 0.710 CausalMutation CLINVAR

dbSNP: rs1168641193
rs1168641193
A 0.700 CausalMutation CLINVAR Bi-allelic POLR3A Loss-of-Function Variants Cause Autosomal-Recessive Wiedemann-Rautenstrauch Syndrome. 30414627

2018

dbSNP: rs1248039821
rs1248039821
A 0.700 GeneticVariation CLINVAR Bi-allelic POLR3A Loss-of-Function Variants Cause Autosomal-Recessive Wiedemann-Rautenstrauch Syndrome. 30414627

2018

dbSNP: rs141484643
rs141484643
T 0.700 CausalMutation CLINVAR Bi-allelic POLR3A Loss-of-Function Variants Cause Autosomal-Recessive Wiedemann-Rautenstrauch Syndrome. 30414627

2018

dbSNP: rs141659018
rs141659018
A 0.700 CausalMutation CLINVAR Bi-allelic POLR3A Loss-of-Function Variants Cause Autosomal-Recessive Wiedemann-Rautenstrauch Syndrome. 30414627

2018

dbSNP: rs1462460124
rs1462460124
C 0.700 CausalMutation CLINVAR Bi-allelic POLR3A Loss-of-Function Variants Cause Autosomal-Recessive Wiedemann-Rautenstrauch Syndrome. 30414627

2018

dbSNP: rs1564613755
rs1564613755
G 0.700 CausalMutation CLINVAR Bi-allelic POLR3A Loss-of-Function Variants Cause Autosomal-Recessive Wiedemann-Rautenstrauch Syndrome. 30414627

2018

dbSNP: rs1564623882
rs1564623882
T 0.700 CausalMutation CLINVAR Bi-allelic POLR3A Loss-of-Function Variants Cause Autosomal-Recessive Wiedemann-Rautenstrauch Syndrome. 30414627

2018

dbSNP: rs181087667
rs181087667
T 0.700 CausalMutation CLINVAR Bi-allelic POLR3A Loss-of-Function Variants Cause Autosomal-Recessive Wiedemann-Rautenstrauch Syndrome. 30414627

2018

dbSNP: rs368905417
rs368905417
T 0.700 CausalMutation CLINVAR Bi-allelic POLR3A Loss-of-Function Variants Cause Autosomal-Recessive Wiedemann-Rautenstrauch Syndrome. 30414627

2018

dbSNP: rs774007232
rs774007232
A 0.700 CausalMutation CLINVAR Bi-allelic POLR3A Loss-of-Function Variants Cause Autosomal-Recessive Wiedemann-Rautenstrauch Syndrome. 30414627

2018

dbSNP: rs1041175828
rs1041175828
T 0.700 CausalMutation CLINVAR

dbSNP: rs1168641193
rs1168641193
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1248039821
rs1248039821
A 0.700 CausalMutation CLINVAR

dbSNP: rs1564612961
rs1564612961
C 0.700 GeneticVariation CLINVAR

dbSNP: rs1564613755
rs1564613755
G 0.700 GeneticVariation CLINVAR

dbSNP: rs1564617848
rs1564617848
C 0.700 CausalMutation CLINVAR

dbSNP: rs1564617848
rs1564617848
C 0.700 GeneticVariation CLINVAR