Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs778361520
rs778361520
A 0.700 GeneticVariation CLINVAR A disease-associated mutation in the adhesion GPCR BAI2 (ADGRB2) increases receptor signaling activity. 28891236

2017

dbSNP: rs387906905
rs387906905
T 0.700 GeneticVariation CLINVAR TRPV4 mutations and cytotoxic hypercalcemia in axonal Charcot-Marie-Tooth neuropathies. 21288981

2011

dbSNP: rs1557055405
rs1557055405
A 0.700 GeneticVariation CLINVAR First missense mutation (W679R) in exon 10 of the adrenoleukodystrophy gene in siblings with adrenomyeloneuropathy. 9452087

1998

dbSNP: rs1057518874
rs1057518874
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1085307993
rs1085307993
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1202430946
rs1202430946
A 0.700 CausalMutation CLINVAR

dbSNP: rs1208636573
rs1208636573
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1247665387
rs1247665387
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1553511224
rs1553511224
TC 0.700 GeneticVariation CLINVAR

dbSNP: rs1555358382
rs1555358382
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1555630216
rs1555630216
T 0.700 CausalMutation CLINVAR

dbSNP: rs1555648288
rs1555648288
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1555727493
rs1555727493
TGGCGGCGGCGGCG 0.700 CausalMutation CLINVAR

dbSNP: rs1555740650
rs1555740650
T 0.700 CausalMutation CLINVAR

dbSNP: rs1556425596
rs1556425596
T 0.700 CausalMutation CLINVAR

dbSNP: rs1559470315
rs1559470315
T 0.700 GeneticVariation CLINVAR

dbSNP: rs201689565
rs201689565
G 0.700 GeneticVariation CLINVAR

dbSNP: rs371334506
rs371334506
G 0.700 CausalMutation CLINVAR

dbSNP: rs61755320
rs61755320
T 0.700 CausalMutation CLINVAR

dbSNP: rs622288
rs622288
T 0.700 GeneticVariation CLINVAR

dbSNP: rs765061840
rs765061840
A 0.700 CausalMutation CLINVAR

dbSNP: rs767350733
rs767350733
A 0.700 CausalMutation CLINVAR

dbSNP: rs864321670
rs864321670
T 0.700 CausalMutation CLINVAR