rs80356740, TARDBP

N. diseases: 2
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.
Familial (FPAH)
CUI: C1611743
Disease: Familial (FPAH)
276 1.000 1 11022556 missense variant A/G snv 1.7E-05 0.010 1.000 1 2008 2008
Neurodegenerative Disorders
CUI: C0524851
Disease: Neurodegenerative Disorders
85 1.000 1 11022556 missense variant A/G snv 1.7E-05 0.010 1.000 1 2008 2008