Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs104894040
rs104894040
SHH
G 0.800 CausalMutation CLINVAR

dbSNP: rs104894040
rs104894040
SHH
C 0.800 CausalMutation CLINVAR

dbSNP: rs104894042
rs104894042
SHH
T 0.800 CausalMutation CLINVAR

dbSNP: rs104894043
rs104894043
SHH
T 0.800 CausalMutation CLINVAR

dbSNP: rs104894048
rs104894048
SHH
C 0.800 CausalMutation CLINVAR

dbSNP: rs104894050
rs104894050
SHH
A 0.800 CausalMutation CLINVAR

dbSNP: rs267607047
rs267607047
SHH
T 0.800 CausalMutation CLINVAR

dbSNP: rs104894044
rs104894044
SHH
A 0.700 CausalMutation CLINVAR

dbSNP: rs104894045
rs104894045
SHH
A 0.700 CausalMutation CLINVAR

dbSNP: rs104894046
rs104894046
SHH
A 0.700 CausalMutation CLINVAR

dbSNP: rs104894051
rs104894051
SHH
A 0.700 CausalMutation CLINVAR

dbSNP: rs104894053
rs104894053
SHH
T 0.700 CausalMutation CLINVAR

dbSNP: rs1057518660
rs1057518660
SHH
T 0.700 CausalMutation CLINVAR

dbSNP: rs121917879
rs121917879
C 0.700 CausalMutation CLINVAR

dbSNP: rs121917880
rs121917880
C 0.700 CausalMutation CLINVAR

dbSNP: rs1347054935
rs1347054935
SHH
0.700 GeneticVariation UNIPROT

dbSNP: rs1420292012
rs1420292012
SHH
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1554493607
rs1554493607
SHH
T 0.700 CausalMutation CLINVAR

dbSNP: rs1554493810
rs1554493810
SHH
C 0.700 CausalMutation CLINVAR

dbSNP: rs1554495331
rs1554495331
SHH
G 0.700 GeneticVariation CLINVAR

dbSNP: rs28936675
rs28936675
SHH
T 0.700 CausalMutation CLINVAR

dbSNP: rs397515375
rs397515375
SHH
T 0.700 CausalMutation CLINVAR

dbSNP: rs397515376
rs397515376
SHH
G 0.700 CausalMutation CLINVAR

dbSNP: rs779093031
rs779093031
SHH
A 0.700 CausalMutation CLINVAR

dbSNP: rs886042458
rs886042458
SHH
A 0.700 CausalMutation CLINVAR