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: rs80338764
rs80338764
2 0.925 9 134824817 missense variant G/C snv 0.800 1.000 5 1997 2009
dbSNP: rs863223458
rs863223458
1 1.000 9 134820143 missense variant G/A snv 0.700 1.000 5 1993 2013
dbSNP: rs764693725
rs764693725
1 1.000 9 134801983 frameshift variant C/-;CC delins 0.700 1.000 2 2012 2013
dbSNP: rs886042173
rs886042173
1 1.000 9 134763738 splice donor variant G/A snv 0.700 1.000 1 2013 2013
dbSNP: rs1057518653
rs1057518653
1 1.000 9 134812622 frameshift variant T/- del 0.700 0
dbSNP: rs1057519596
rs1057519596
1 1.000 9 134767320 frameshift variant -/C delins 0.700 0
dbSNP: rs1060502242
rs1060502242
1 1.000 9 134691028 frameshift variant AG/- delins 0.700 0
dbSNP: rs1060502248
rs1060502248
1 1.000 9 134780147 splice donor variant G/A snv 0.700 0
dbSNP: rs1060502250
rs1060502250
1 1.000 9 134834973 inframe deletion CCT/- delins 0.700 0
dbSNP: rs1060502255
rs1060502255
1 1.000 9 134817803 frameshift variant A/- delins 0.700 0
dbSNP: rs1060502258
rs1060502258
1 1.000 9 134767009 stop gained G/T snv 0.700 0
dbSNP: rs1060502259
rs1060502259
1 1.000 9 134818655 splice region variant G/- delins 0.700 0
dbSNP: rs1179967153
rs1179967153
1 1.000 9 134796895 frameshift variant C/- delins 0.700 0
dbSNP: rs121912932
rs121912932
2 0.925 0.160 9 134820135 missense variant G/A snv 0.700 0
dbSNP: rs121912933
rs121912933
1 1.000 9 134774901 stop gained C/T snv 0.700 0
dbSNP: rs1554726279
rs1554726279
1 1.000 9 134835132 frameshift variant C/- delins 0.700 0
dbSNP: rs1554792869
rs1554792869
1 1.000 9 134754279 stop gained C/T snv 0.700 0
dbSNP: rs1554803622
rs1554803622
1 1.000 9 134805159 splice region variant -/G delins 0.700 0
dbSNP: rs1554805142
rs1554805142
1 1.000 9 134812665 stop gained C/T snv 0.700 0
dbSNP: rs1554807812
rs1554807812
1 1.000 9 134823427 frameshift variant CCCGA/- del 0.700 0
dbSNP: rs1564418237
rs1564418237
1 1.000 9 134732099 frameshift variant A/- delins 0.700 0
dbSNP: rs1564453831
rs1564453831
1 1.000 9 134780099 splice region variant C/G snv 0.700 0
dbSNP: rs1564481053
rs1564481053
1 1.000 9 134818764 splice donor variant G/A snv 0.700 0
dbSNP: rs183495554
rs183495554
1 1.000 9 134834960 intron variant T/A;C snv 1.4E-03 0.700 0
dbSNP: rs35002351
rs35002351
1 1.000 9 134812604 splice region variant G/- delins 0.700 0