rs121918094, TTR

N. diseases: 8
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.
Liver carcinoma
CUI: C2239176
Disease: Liver carcinoma
942 0.827 0.280 18 31592921 missense variant T/C snv 0.010 1.000 1 2013 2013
Liver neoplasms
CUI: C0023903
Disease: Liver neoplasms
7 0.827 0.280 18 31592921 missense variant T/C snv 0.010 1.000 1 2013 2013
Peripheral Nervous System Diseases
CUI: C4721453
Disease: Peripheral Nervous System Diseases
69 0.827 0.280 18 31592921 missense variant T/C snv 0.010 1.000 1 2013 2013
Peripheral Neuropathy
CUI: C0031117
Disease: Peripheral Neuropathy
81 0.827 0.280 18 31592921 missense variant T/C snv 0.010 1.000 1 2013 2013
Sepsis
CUI: C0243026
Disease: Sepsis
144 0.827 0.280 18 31592921 missense variant T/C snv 0.010 1.000 1 2010 2010
Septicemia
CUI: C0036690
Disease: Septicemia
141 0.827 0.280 18 31592921 missense variant T/C snv 0.010 1.000 1 2010 2010
Amyloidosis
CUI: C0002726
Disease: Amyloidosis
93 0.827 0.280 18 31592921 missense variant T/C snv 0.030 1.000 3 1999 2015
AMYLOIDOSIS, HEREDITARY, TRANSTHYRETIN-RELATED
CUI: C2751492
Disease: AMYLOIDOSIS, HEREDITARY, TRANSTHYRETIN-RELATED
68 0.827 0.280 18 31592921 missense variant T/C snv 0.800 1.000 22 1986 2014