rs557327165, HSPB1

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.
CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2F
CUI: C1847823
Disease: CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2F
15 0.925 0.080 7 76302828 missense variant C/G;T snv 4.4E-06 0.800 1.000 6 2004 2015
NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE IIB
CUI: C2608087
Disease: NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE IIB
17 0.925 0.080 7 76302828 missense variant C/G;T snv 4.4E-06 0.700 1.000 11 2004 2017
Neuropathy
CUI: C0442874
Disease: Neuropathy
110 0.925 0.080 7 76302828 missense variant C/G;T snv 4.4E-06 0.010 1.000 1 2015 2015