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: rs387906225
rs387906225
1 1.000 0.080 9 101428485 frameshift variant TGTT/- delins 7.0E-05 0.700 1.000 12 1990 2015
dbSNP: rs1554702433
rs1554702433
1 1.000 0.080 9 101425566 missense variant A/G snv 0.700 1.000 11 1988 2010
dbSNP: rs1554702442
rs1554702442
1 1.000 0.080 9 101425588 missense variant C/A snv 0.700 1.000 11 1988 2010
dbSNP: rs370793608
rs370793608
1 1.000 0.080 9 101426567 stop gained A/C;T snv 7.0E-06 0.700 1.000 7 1993 2012
dbSNP: rs786204503
rs786204503
1 1.000 0.080 9 101425629 splice acceptor variant T/C snv 0.700 1.000 3 2004 2012
dbSNP: rs1057516534
rs1057516534
1 1.000 0.080 9 101430775 splice donor variant C/- delins 0.700 1.000 1 2015 2015
dbSNP: rs1057516902
rs1057516902
1 1.000 0.080 9 101427578 stop gained C/T snv 0.700 1.000 1 2008 2008
dbSNP: rs1554702328
rs1554702328
1 1.000 0.080 9 101424901 splice acceptor variant -/A delins 0.700 1.000 1 2012 2012
dbSNP: rs1554702666
rs1554702666
1 1.000 0.080 9 101427643 splice acceptor variant C/T snv 0.700 1.000 1 2015 2015
dbSNP: rs181639417
rs181639417
1 1.000 0.080 9 101435708 splice donor variant C/G snv 0.700 1.000 1 2010 2010
dbSNP: rs1057516379
rs1057516379
1 1.000 0.080 9 101429753 splice donor variant A/T snv 0.700 0
dbSNP: rs1057517091
rs1057517091
1 1.000 0.080 9 101426633 frameshift variant T/- del 0.700 0
dbSNP: rs1057517133
rs1057517133
1 1.000 0.080 9 101424954 stop gained C/T snv 0.700 0
dbSNP: rs118204425
rs118204425
1 1.000 0.080 9 101424975 inframe deletion AAG/- del 0.700 0
dbSNP: rs118204426
rs118204426
1 1.000 0.080 9 101425532 stop gained G/T snv 0.700 0
dbSNP: rs1300461861
rs1300461861
1 1.000 0.080 9 101427644 splice acceptor variant T/C;G snv 7.0E-06 0.700 0
dbSNP: rs1402966846
rs1402966846
1 1.000 0.080 9 101428524 splice acceptor variant C/T snv 0.700 0
dbSNP: rs1554702325
rs1554702325
1 1.000 0.080 9 101424901 splice acceptor variant C/T snv 0.700 0
dbSNP: rs1554702353
rs1554702353
1 1.000 0.080 9 101425030 frameshift variant A/- delins 0.700 0
dbSNP: rs1554702425
rs1554702425
1 1.000 0.080 9 101425539 frameshift variant -/G delins 0.700 0
dbSNP: rs1554702890
rs1554702890
1 1.000 0.080 9 101429792 frameshift variant T/- delins 0.700 0
dbSNP: rs1564077542
rs1564077542
1 1.000 0.080 9 101425628 splice acceptor variant C/T snv 0.700 0
dbSNP: rs387906226
rs387906226
1 1.000 0.080 9 101426626 inframe deletion ACCAGT/- delins 0.700 0
dbSNP: rs781023784
rs781023784
1 1.000 0.080 9 101429858 missense variant A/G snv 4.0E-06 0.700 1.000 11 1988 2010
dbSNP: rs764701775
rs764701775
1 1.000 0.080 9 101425482 missense variant A/G snv 4.0E-06 0.700 1.000 11 1988 2010