Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs79781594
rs79781594
0.732 0.160 10 43113649 missense variant G/A;C;T snv
CUI: C0342190
Disease: C-cell hyperplasia of thyroid
C-cell hyperplasia of thyroid
Pathological Conditions, Signs and Symptoms; Endocrine System Diseases 0.030 1.000 3 2013 2019