rs2732260, FUT10

N. diseases: 5
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.
Amnesia
CUI: C0002622
Disease: Amnesia
12 0.882 0.200 8 33431749 intron variant G/A snv 8.4E-02 0.700 1.000 1 2018 2018
Frontotemporal dementia
CUI: C0338451
Disease: Frontotemporal dementia
215 0.882 0.200 8 33431749 intron variant G/A snv 8.4E-02 0.700 1.000 1 2018 2018
Memory dysfunction
CUI: C3887551
Disease: Memory dysfunction
3 0.882 0.200 8 33431749 intron variant G/A snv 8.4E-02 0.700 1.000 1 2018 2018
Memory impairment
CUI: C0233794
Disease: Memory impairment
48 0.882 0.200 8 33431749 intron variant G/A snv 8.4E-02 0.700 1.000 1 2018 2018
Memory Impairment, CTCAE 3.0
CUI: C1963167
Disease: Memory Impairment, CTCAE 3.0
2 0.882 0.200 8 33431749 intron variant G/A snv 8.4E-02 0.700 1.000 1 2018 2018