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: rs1057519074
rs1057519074
MSN
1 1.000 X 65731150 missense variant C/T snv 0.800 1.000 3 2016 2018
dbSNP: rs1057519075
rs1057519075
MSN
1 1.000 X 65739816 stop gained C/T snv 0.700 0