rs1563518388, PMP2

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.
CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 1G
CUI: C4748940
Disease: CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 1G
3 1.000 8 81444908 missense variant A/G snv 0.700 0
Peripheral Neuropathy
CUI: C0031117
Disease: Peripheral Neuropathy
81 1.000 8 81444908 missense variant A/G snv 0.700 0