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: rs1562173313
rs1562173313
QRSL1
1 1.000 6 106663098 missense variant GC/TT mnv 0.700 1.000 1 2018 2018