rs587777789, TFG

N. diseases: 3
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.
Neuropathy, hereditary motor and sensory, Okinawa type
CUI: C1858338
Disease: Neuropathy, hereditary motor and sensory, Okinawa type
2 0.882 0.080 3 100744917 missense variant G/A;T snv 4.0E-06 0.700 0
Charcot-Marie-Tooth Disease
CUI: C0007959
Disease: Charcot-Marie-Tooth Disease
136 0.882 0.080 3 100744917 missense variant G/A;T snv 4.0E-06 0.010 1.000 1 2019 2019
Hereditary Motor and Sensory-Neuropathy Type II
CUI: C0270914
Disease: Hereditary Motor and Sensory-Neuropathy Type II
144 0.882 0.080 3 100744917 missense variant G/A;T snv 4.0E-06 0.010 1.000 1 2016 2016