Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121434309
rs121434309
Entrez Id: 5925;10161
Gene Symbol: RB1;LPAR6
RB1;LPAR6
CUI: C3279470
Disease:
HYPOTRICHOSIS 8
0.800 GeneticVariation UNIPROT Disruption of P2RY5, an orphan G protein-coupled receptor, underlies autosomal recessive woolly hair. 18297072 2008
dbSNP: rs121434309
rs121434309
Entrez Id: 5925;10161
Gene Symbol: RB1;LPAR6
RB1;LPAR6
CUI: C3279470
Disease:
HYPOTRICHOSIS 8
T 0.800 CausalMutation CLINVAR