Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs201249971
rs201249971
0.010 GeneticVariation BEFREE Homozygotes for the LIPH c.736T>A (p.C246S) mutation, the most prevalent genotype in Japanese patients, present varying degrees of hair loss; however, determinants of this phenotypic diversity remain elusive. 27375176

2017

dbSNP: rs201868115
rs201868115
0.010 GeneticVariation BEFREE The severe phenotype of complete baldness was seen in only 1 patient with homozygous c.742C>A. 24586639

2014