rs150794546, BRD2

N. diseases: 1
Disease: Hypothyroidism ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Hypothyroidism
CUI: C0020676
Disease: Hypothyroidism
0.010 GeneticVariation BEFREE Sequencing of the entire coding region the FSH gene revealed wild-type alleles for all the known mutations, and the A919G and A2039G polymorphisms, previously associated with good response to FSH stimulation and severe iatrogenic OHSS.We ruled out hypothyroidism. 18166181 2008