rs1565869918, FGD4

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.
Abnormal peripheral nervous system morphology
CUI: C4025831
Disease: Abnormal peripheral nervous system morphology
2 0.882 0.120 12 32582378 frameshift variant G/- delins 0.700 0
CHARCOT-MARIE-TOOTH DISEASE, TYPE 4H
CUI: C1836336
Disease: CHARCOT-MARIE-TOOTH DISEASE, TYPE 4H
8 0.882 0.120 12 32582378 frameshift variant G/- delins 0.700 0
Peripheral demyelinating neuropathy
CUI: C0270922
Disease: Peripheral demyelinating neuropathy
14 0.882 0.120 12 32582378 frameshift variant G/- delins 0.700 0