Source: BEFREE

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1554927408
rs1554927408
FGFR2
CUI: C0027962
Disease: Melanocytic nevus
Melanocytic nevus 		0.010 GeneticVariation BEFREE A similar paralogous missense mutation in the transmembrane domain of FGFR3 (p.Gly380Arg) has been reported in keratinocytic epidermal naevi. 27095246

2017