rs1405183655, FA2H

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.
Muscle Weakness
CUI: C0151786
Disease: Muscle Weakness
87 16 74719132 missense variant C/G;T snv 4.0E-06 0.010 1.000 1 2017 2017
Paresis
CUI: C0030552
Disease: Paresis
49 16 74719132 missense variant C/G;T snv 4.0E-06 0.010 1.000 1 2017 2017