rs750174047, DNAH8

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.
Cap Myopathy
CUI: C3710589
Disease: Cap Myopathy
4 1.000 0.080 6 38722964 missense variant A/T snv 8.2E-06 0.010 1.000 1 2018 2018
Muscle Weakness
CUI: C0151786
Disease: Muscle Weakness
87 1.000 0.080 6 38722964 missense variant A/T snv 8.2E-06 0.010 1.000 1 2019 2019
Paresis
CUI: C0030552
Disease: Paresis
49 1.000 0.080 6 38722964 missense variant A/T snv 8.2E-06 0.010 1.000 1 2019 2019