rs879253869, PMP2

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, DEMYELINATING, TYPE 1G
3 0.925 0.080 8 81444935 missense variant A/T snv 0.800 1.000 4 2015 2018
Peripheral Neuropathy
CUI: C0031117
Disease: Peripheral Neuropathy
81 0.925 0.080 8 81444935 missense variant A/T snv 0.700 1.000 1 2015 2015
Charcot-Marie-Tooth Disease
CUI: C0007959
Disease: Charcot-Marie-Tooth Disease
136 0.925 0.080 8 81444935 missense variant A/T snv 0.020 1.000 2 2016 2019