Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs786204790
rs786204790
TSHR ; LOC101928462
C 0.700 GeneticVariation CLINVAR The Italian screening program for primary congenital hypothyroidism: actions to improve screening, diagnosis, follow-up, and surveillance. 23404215

2013