Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121912530
rs121912530
LHCGR ; GTF2A1L ; STON1-GTF2A1L
0.010 GeneticVariation BEFREE In a patient with micropenis, the analysis revealed a homozygous missense mutation at codon 625 (I625K). 11849253

2002