rs879253863, TRIM2

N. diseases: 4
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.
CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2R
CUI: C3809655
Disease: CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2R
4 0.925 0.160 4 153324126 missense variant A/C snv 0.700 1.000 2 2015 2015
Bilateral vocal cord paralysis
CUI: C2146481
Disease: Bilateral vocal cord paralysis
2 0.925 0.160 4 153324126 missense variant A/C snv 0.010 1.000 1 2015 2015
Peripheral Nervous System Diseases
CUI: C4721453
Disease: Peripheral Nervous System Diseases
69 0.925 0.160 4 153324126 missense variant A/C snv 0.010 1.000 1 2015 2015
Peripheral Neuropathy
CUI: C0031117
Disease: Peripheral Neuropathy
81 0.925 0.160 4 153324126 missense variant A/C snv 0.010 1.000 1 2015 2015