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: rs137853035
rs137853035
DYNC2H1
1 1.000 0.080 11 103177640 missense variant A/G snv 0.800 1.000 4 2009 2013