rs201868115, LIPH

N. diseases: 3
Disease: Alopecia ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Alopecia
CUI: C0002170
Disease: Alopecia
0.010 GeneticVariation BEFREE The severe phenotype of complete baldness was seen in only 1 patient with homozygous c.742C>A. 24586639 2014