rs137853162, THRA

N. diseases: 1
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 6
CUI: C3280817
Disease: HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 6
7 1.000 17 40077520 missense variant G/T snv 0.700 0