Source: ALL
Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs138890576
rs138890576
DNAH5
4 0.882 0.160 5 13844931 missense variant A/G snv 1.2E-05 7.0E-06 0.700 1.000 1 2016 2016
dbSNP: rs770861172
rs770861172
DNAH7
6 0.827 0.160 2 195857582 missense variant C/T snv 4.0E-06 7.0E-06 0.700 0