rs121918070, TTR

N. diseases: 2
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.
AMYLOIDOSIS, HEREDITARY, TRANSTHYRETIN-RELATED
CUI: C2751492
Disease: AMYLOIDOSIS, HEREDITARY, TRANSTHYRETIN-RELATED
68 1.000 0.120 18 31595157 missense variant A/G snv 4.0E-06 1.4E-05 0.800 1.000 39 1986 2015
Cardiomyopathies
CUI: C0878544
Disease: Cardiomyopathies
294 1.000 0.120 18 31595157 missense variant A/G snv 4.0E-06 1.4E-05 0.700 0