Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs587778792
rs587778792
SHH
G 0.710 CausalMutation CLINVAR

dbSNP: rs587778799
rs587778799
SHH
G 0.710 CausalMutation CLINVAR

dbSNP: rs104894040
rs104894040
SHH
G 0.700 CausalMutation CLINVAR

dbSNP: rs104894040
rs104894040
SHH
C 0.700 CausalMutation CLINVAR

dbSNP: rs104894042
rs104894042
SHH
T 0.700 CausalMutation CLINVAR

dbSNP: rs104894043
rs104894043
SHH
T 0.700 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: rs104894048
rs104894048
SHH
C 0.700 CausalMutation CLINVAR

dbSNP: rs104894050
rs104894050
SHH
A 0.700 CausalMutation CLINVAR

dbSNP: rs104894051
rs104894051
SHH
A 0.700 CausalMutation CLINVAR

dbSNP: rs139565972
rs139565972
A 0.700 GeneticVariation CLINVAR

dbSNP: rs146990376
rs146990376
SHH
C 0.700 CausalMutation CLINVAR

dbSNP: rs1490604080
rs1490604080
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1554834321
rs1554834321
A 0.700 CausalMutation CLINVAR

dbSNP: rs1554834889
rs1554834889
G 0.700 GeneticVariation CLINVAR

dbSNP: rs1554834892
rs1554834892
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1557612048
rs1557612048
C 0.700 GeneticVariation CLINVAR

dbSNP: rs267607047
rs267607047
SHH
T 0.700 CausalMutation CLINVAR

dbSNP: rs28936675
rs28936675
SHH
T 0.700 CausalMutation CLINVAR

dbSNP: rs397515364
rs397515364
GC 0.700 CausalMutation CLINVAR

dbSNP: rs397515365
rs397515365
T 0.700 CausalMutation CLINVAR

dbSNP: rs397515375
rs397515375
SHH
T 0.700 CausalMutation CLINVAR

dbSNP: rs397515376
rs397515376
SHH
G 0.700 CausalMutation CLINVAR