Source: CURATED ×
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1565623093
rs1565623093
0.700 CausalMutation CLINVAR

dbSNP: rs76992529
rs76992529
TTR
A 0.780 CausalMutation CLINVAR

dbSNP: rs1024095026
rs1024095026
A 0.700 GeneticVariation CLINVAR Pancreatic cancer genomes reveal aberrations in axon guidance pathway genes. 23103869

2012

dbSNP: rs114638163
rs114638163
A 0.700 CausalMutation CLINVAR MIPEP recessive variants cause a syndrome of left ventricular non-compaction, hypotonia, and infantile death. 27799064

2016

dbSNP: rs121912998
rs121912998
A 0.700 CausalMutation CLINVAR Postmortem genetic screening for the identification, verification, and reporting of genetic variants contributing to the sudden death of the young. 27435932

2016

dbSNP: rs1242465339
rs1242465339
A 0.700 CausalMutation CLINVAR

dbSNP: rs141735183
rs141735183
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1425855043
rs1425855043
A 0.700 CausalMutation CLINVAR

dbSNP: rs148515772
rs148515772
EMD
A 0.700 GeneticVariation CLINVAR

dbSNP: rs148808089
rs148808089
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1553644307
rs1553644307
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1553663867
rs1553663867
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1559873786
rs1559873786
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1561698362
rs1561698362
DSP
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1564526327
rs1564526327
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1565050709
rs1565050709
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1565590176
rs1565590176
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1565590309
rs1565590309
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1565627110
rs1565627110
A 0.700 CausalMutation CLINVAR

dbSNP: rs193922683
rs193922683
A 0.700 GeneticVariation CLINVAR

dbSNP: rs193922708
rs193922708
A 0.700 GeneticVariation CLINVAR

dbSNP: rs267607004
rs267607004
A 0.700 CausalMutation CLINVAR

dbSNP: rs267607571
rs267607571
A 0.700 CausalMutation CLINVAR

dbSNP: rs28933979
rs28933979
TTR
A 0.700 CausalMutation CLINVAR

dbSNP: rs371678190
rs371678190
A 0.700 CausalMutation CLINVAR