Source: CURATED

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs76992529
rs76992529
TTR
0.653 0.560 18 31598655 missense variant G/A snv 1.1E-03 4.9E-03
AMYLOIDOSIS, HEREDITARY, TRANSTHYRETIN-RELATED
0.860 1.000 39 1986 2019
dbSNP: rs76992529
rs76992529
TTR
0.653 0.560 18 31598655 missense variant G/A snv 1.1E-03 4.9E-03
CUI: C0878544
Disease: Cardiomyopathies
Cardiomyopathies
0.780 1.000 0 2001 2019
dbSNP: rs76992529
rs76992529
TTR
0.653 0.560 18 31598655 missense variant G/A snv 1.1E-03 4.9E-03
CUI: C0007286
Disease: Carpal Tunnel Syndrome
Carpal Tunnel Syndrome
0.710 1.000 0 2019 2019
dbSNP: rs76992529
rs76992529
TTR
0.653 0.560 18 31598655 missense variant G/A snv 1.1E-03 4.9E-03
CUI: C0002871
Disease: Anemia
Anemia
0.700 0
dbSNP: rs76992529
rs76992529
TTR
0.653 0.560 18 31598655 missense variant G/A snv 1.1E-03 4.9E-03
CUI: C0030312
Disease: Pancytopenia
Pancytopenia
0.700 0
dbSNP: rs76992529
rs76992529
TTR
0.653 0.560 18 31598655 missense variant G/A snv 1.1E-03 4.9E-03
AMYLOID CARDIOMYOPATHY, TRANSTHYRETIN-RELATED
0.700 0
dbSNP: rs76992529
rs76992529
TTR
0.653 0.560 18 31598655 missense variant G/A snv 1.1E-03 4.9E-03
Transthyretin related familial amyloid cardiomyopathy
0.700 0
dbSNP: rs76992529
rs76992529
TTR
0.653 0.560 18 31598655 missense variant G/A snv 1.1E-03 4.9E-03
CUI: C1855710
Disease: Bone marrow hypocellularity
Bone marrow hypocellularity
0.700 0
dbSNP: rs76992529
rs76992529
TTR
0.653 0.560 18 31598655 missense variant G/A snv 1.1E-03 4.9E-03
Dystransthyretinemic Euthyroidal Hyperthyroxinemia
0.700 0
dbSNP: rs76992529
rs76992529
TTR
0.653 0.560 18 31598655 missense variant G/A snv 1.1E-03 4.9E-03
CUI: C0032285
Disease: Pneumonia
Pneumonia
0.700 0