rs1184021143, SLC25A46

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.
NEUROPATHY, HEREDITARY MOTOR AND SENSORY, TYPE VIB
CUI: C4225302
Disease: NEUROPATHY, HEREDITARY MOTOR AND SENSORY, TYPE VIB
11 0.925 0.080 5 110761295 missense variant G/A snv 4.0E-06 0.700 0
Optic Atrophy
CUI: C0029124
Disease: Optic Atrophy
51 0.925 0.080 5 110761295 missense variant G/A snv 4.0E-06 0.700 0