Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1425998598
rs1425998598
A 0.700 GeneticVariation CLINVAR Haploinsufficiency of the Chromatin Remodeler BPTF Causes Syndromic Developmental and Speech Delay, Postnatal Microcephaly, and Dysmorphic Features. 28942966

2017

dbSNP: rs1057518083
rs1057518083
T 0.700 CausalMutation CLINVAR

dbSNP: rs1057518871
rs1057518871
G 0.700 GeneticVariation CLINVAR

dbSNP: rs1057518879
rs1057518879
A 0.700 CausalMutation CLINVAR

dbSNP: rs1057518909
rs1057518909
C 0.700 CausalMutation CLINVAR

dbSNP: rs1057519389
rs1057519389
T 0.700 CausalMutation CLINVAR

dbSNP: rs1085307845
rs1085307845
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1085307993
rs1085307993
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1085308004
rs1085308004
G 0.700 CausalMutation CLINVAR

dbSNP: rs111854391
rs111854391
T 0.700 CausalMutation CLINVAR

dbSNP: rs112550005
rs112550005
A 0.700 CausalMutation CLINVAR

dbSNP: rs113812345
rs113812345
A 0.700 CausalMutation CLINVAR

dbSNP: rs121918467
rs121918467
T 0.700 CausalMutation CLINVAR

dbSNP: rs1232880706
rs1232880706
A 0.700 CausalMutation CLINVAR

dbSNP: rs1276519904
rs1276519904
G 0.700 GeneticVariation CLINVAR

dbSNP: rs137854461
rs137854461
C 0.700 CausalMutation CLINVAR

dbSNP: rs137854466
rs137854466
A 0.700 CausalMutation CLINVAR

dbSNP: rs142239530
rs142239530
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1443187318
rs1443187318
TA 0.700 CausalMutation CLINVAR

dbSNP: rs1553517323
rs1553517323
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1554700718
rs1554700718
C 0.700 GeneticVariation CLINVAR

dbSNP: rs1554726245
rs1554726245
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1555398397
rs1555398397
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1555398673
rs1555398673
G 0.700 CausalMutation CLINVAR

dbSNP: rs1555572254
rs1555572254
C 0.700 CausalMutation CLINVAR