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: rs369614706
rs369614706
DYNC2H1
1 1.000 0.080 11 103120705 missense variant C/T snv 2.4E-05 3.5E-05 0.010 1.000 1 2015 2015
dbSNP: rs752449341
rs752449341
DYNC2H1
1 1.000 0.080 11 103220686 missense variant C/T snv 1.2E-05 1.4E-05 0.010 1.000 1 2015 2015