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: rs878853141
rs878853141
1 1.000 0.200 X 53199068 missense variant C/G snv 0.700 0
dbSNP: rs878853151
rs878853151
1 1.000 0.200 X 53211601 frameshift variant -/A delins 0.700 0