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: rs863224910
rs863224910
1 1.000 8 116847588 missense variant A/G snv 0.700 0
dbSNP: rs1563686762
rs1563686762
16 0.790 0.280 8 116847620 inframe deletion GTT/- delins 0.700 1.000 1 2019 2019
dbSNP: rs387907213
rs387907213
1 1.000 8 116847643 missense variant A/G snv 0.800 1.000 1 2012 2012
dbSNP: rs1563687901
rs1563687901
1 1.000 8 116850687 frameshift variant -/G delins 0.700 1.000 1 2019 2019
dbSNP: rs1563689416
rs1563689416
1 1.000 8 116854244 splice donor variant C/T snv 0.700 1.000 1 2019 2019
dbSNP: rs387907212
rs387907212
1 1.000 8 116854279 missense variant G/C snv 0.800 1.000 1 2012 2012
dbSNP: rs797045909
rs797045909
1 1.000 8 116857361 frameshift variant -/CT delins 0.700 0
dbSNP: rs797045908
rs797045908
1 1.000 8 116857375 frameshift variant -/T delins 0.700 0
dbSNP: rs1554612093
rs1554612093
1 1.000 8 116863196 stop gained T/A snv 0.700 0
dbSNP: rs1554612096
rs1554612096
1 1.000 8 116863221 frameshift variant -/AG delins 0.700 0
dbSNP: rs797045907
rs797045907
1 1.000 8 116866668 frameshift variant GCTAGCC/- delins 0.700 0