Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1555682265
rs1555682265
DCC
T 0.700 CausalMutation CLINVAR Biallelic mutations in human DCC cause developmental split-brain syndrome. 28250456

2017

dbSNP: rs1057516033
rs1057516033
A 0.700 CausalMutation CLINVAR A prospective evaluation of whole-exome sequencing as a first-tier molecular test in infants with suspected monogenic disorders. 26938784

2016

dbSNP: rs750610248
rs750610248
C 0.700 CausalMutation CLINVAR Multisystem Anomalies in Severe Combined Immunodeficiency with Mutant BCL11B. 27959755

2016

dbSNP: rs1057517858
rs1057517858
T 0.700 CausalMutation CLINVAR

dbSNP: rs1057518951
rs1057518951
T 0.700 CausalMutation CLINVAR

dbSNP: rs1057519053
rs1057519053
DCC
T 0.700 CausalMutation CLINVAR

dbSNP: rs1057519054
rs1057519054
DCC
G 0.700 CausalMutation CLINVAR

dbSNP: rs1057519055
rs1057519055
DCC
A 0.700 CausalMutation CLINVAR

dbSNP: rs1057519056
rs1057519056
DCC
C 0.700 CausalMutation CLINVAR

dbSNP: rs1057519057
rs1057519057
DCC
A 0.700 CausalMutation CLINVAR

dbSNP: rs1057523157
rs1057523157
A 0.700 CausalMutation CLINVAR

dbSNP: rs1064796460
rs1064796460
G 0.700 CausalMutation CLINVAR

dbSNP: rs1555155556
rs1555155556
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1555380716
rs1555380716
GC 0.700 GeneticVariation CLINVAR

dbSNP: rs1555696625
rs1555696625
A 0.700 CausalMutation CLINVAR

dbSNP: rs1558519119
rs1558519119
A 0.700 CausalMutation CLINVAR

dbSNP: rs1563183469
rs1563183469
C 0.700 GeneticVariation CLINVAR

dbSNP: rs1563406024
rs1563406024
GA 0.700 GeneticVariation CLINVAR

dbSNP: rs1565627707
rs1565627707
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1569234334
rs1569234334
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1569459580
rs1569459580
A 0.700 GeneticVariation CLINVAR

dbSNP: rs199651452
rs199651452
DCC
T 0.700 CausalMutation CLINVAR

dbSNP: rs431905509
rs431905509
A 0.700 GeneticVariation CLINVAR

dbSNP: rs750195040
rs750195040
A 0.700 GeneticVariation CLINVAR

dbSNP: rs754914260
rs754914260
DCC
T 0.700 CausalMutation CLINVAR