Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs139455627
rs139455627
TSPEAR
A 0.700 GeneticVariation CLINVAR Mutations in TSPEAR, Encoding a Regulator of Notch Signaling, Affect Tooth and Hair Follicle Morphogenesis. 27736875

2016
dbSNP: rs1569151872
rs1569151872
TSPEAR-AS1 ; TSPEAR
AA 0.700 GeneticVariation CLINVAR Mutations in TSPEAR, Encoding a Regulator of Notch Signaling, Affect Tooth and Hair Follicle Morphogenesis. 27736875

2016
dbSNP: rs149830411
rs149830411
KANSL1
A 0.700 CausalMutation CLINVAR

dbSNP: rs1553655558
rs1553655558
TRIP12
G 0.700 CausalMutation CLINVAR

dbSNP: rs1559759089
rs1559759089
ATP6V1A
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1565706229
rs1565706229
EED ; MIR6755
C 0.700 GeneticVariation CLINVAR

dbSNP: rs267606670
rs267606670
ATP1A3
T 0.700 CausalMutation CLINVAR

dbSNP: rs387907141
rs387907141
ARID1B
T 0.700 CausalMutation CLINVAR

dbSNP: rs398123009
rs398123009
PACS1
T 0.700 CausalMutation CLINVAR

dbSNP: rs796052243
rs796052243
SPATA5
T 0.700 GeneticVariation CLINVAR