rs11541796, TTR

N. diseases: 9
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 0.807 0.280 18 31593011 missense variant A/G snv 0.810 1.000 3 1994 2014
Adenomatous Polyposis Coli
CUI: C0032580
Disease: Adenomatous Polyposis Coli
237 0.807 0.280 18 31593011 missense variant A/G snv 0.010 1.000 1 1994 1994
Amyloidosis
CUI: C0002726
Disease: Amyloidosis
93 0.807 0.280 18 31593011 missense variant A/G snv 0.010 1.000 1 1994 1994
Bilateral carpal tunnel syndrome
CUI: C3864035
Disease: Bilateral carpal tunnel syndrome
2 0.807 0.280 18 31593011 missense variant A/G snv 0.010 1.000 1 2007 2007
Cardiomyopathies
CUI: C0878544
Disease: Cardiomyopathies
294 0.807 0.280 18 31593011 missense variant A/G snv 0.010 1.000 1 2007 2007
Peripheral Nervous System Diseases
CUI: C4721453
Disease: Peripheral Nervous System Diseases
69 0.807 0.280 18 31593011 missense variant A/G snv 0.010 1.000 1 2007 2007
Peripheral Neuropathy
CUI: C0031117
Disease: Peripheral Neuropathy
81 0.807 0.280 18 31593011 missense variant A/G snv 0.010 1.000 1 2007 2007
Polyneuropathy
CUI: C0152025
Disease: Polyneuropathy
32 0.807 0.280 18 31593011 missense variant A/G snv 0.010 1.000 1 1990 1990
Senile cardiac amyloidosis
CUI: C0268407
Disease: Senile cardiac amyloidosis
19 0.807 0.280 18 31593011 missense variant A/G snv 0.010 1.000 1 1998 1998