rs370579379, RBP4;FFAR4

N. diseases: 6
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
CUI: C0002726
Disease: Amyloidosis
93 0.827 0.160 10 93594018 missense variant C/T snv 4.0E-06 1.4E-05 0.010 1.000 1 2017 2017
Carpal Tunnel Syndrome
CUI: C0007286
Disease: Carpal Tunnel Syndrome
46 0.827 0.160 10 93594018 missense variant C/T snv 4.0E-06 1.4E-05 0.010 1.000 1 2019 2019
Congestive heart failure
CUI: C0018802
Disease: Congestive heart failure
165 0.827 0.160 10 93594018 missense variant C/T snv 4.0E-06 1.4E-05 0.010 1.000 1 2017 2017
Heart failure
CUI: C0018801
Disease: Heart failure
201 0.827 0.160 10 93594018 missense variant C/T snv 4.0E-06 1.4E-05 0.010 1.000 1 2017 2017
Mononeuropathies
CUI: C0494491
Disease: Mononeuropathies
2 0.827 0.160 10 93594018 missense variant C/T snv 4.0E-06 1.4E-05 0.010 1.000 1 2019 2019
Transthyretin cardiac amyloidosis
CUI: C4531196
Disease: Transthyretin cardiac amyloidosis
2 0.827 0.160 10 93594018 missense variant C/T snv 4.0E-06 1.4E-05 0.010 1.000 1 2017 2017