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: rs375759781
rs375759781
1 13 20189108 stop gained G/A;C snv 1.2E-05 0.700 0
dbSNP: rs587783645
rs587783645
2 1.000 0.120 13 20189424 missense variant C/A;T snv 0.700 0
dbSNP: rs587783646
rs587783646
2 1.000 0.120 13 20188949 frameshift variant CA/- delins 4.0E-06 0.700 0
dbSNP: rs587783647
rs587783647
3 0.925 0.120 13 20188932 frameshift variant TCTA/- delins 4.8E-05 2.1E-05 0.700 0
dbSNP: rs756484720
rs756484720
2 1.000 0.120 13 20189247 frameshift variant TT/- delins 8.0E-06 1.4E-05 0.700 0
dbSNP: rs76434661
rs76434661
11 0.763 0.280 13 20189166 missense variant C/T snv 2.9E-04 4.6E-04 0.700 0
dbSNP: rs786204734
rs786204734
2 1.000 0.120 13 20192783 splice region variant C/A;T snv 0.700 0
dbSNP: rs80338939
rs80338939
14 0.732 0.280 13 20189547 frameshift variant C/-;CC delins 6.4E-03 0.700 0
dbSNP: rs80338940
rs80338940
11 0.763 0.280 13 20192782 splice donor variant C/T snv 2.3E-04 0.700 0
dbSNP: rs80338942
rs80338942
10 0.776 0.280 13 20189415 frameshift variant A/- del 8.9E-04 5.8E-04 0.700 0
dbSNP: rs80338943
rs80338943
6 0.851 0.120 13 20189347 frameshift variant G/- delins 4.7E-04; 4.0E-06 2.1E-04 0.700 0
dbSNP: rs80338947
rs80338947
3 1.000 0.120 13 20189222 inframe deletion CTC/- delins 7.2E-05 9.1E-05 0.700 0
dbSNP: rs998045226
rs998045226
2 1.000 0.120 13 20189032 missense variant G/A snv 1.2E-05 2.8E-05 0.700 0
dbSNP: rs2274083
rs2274083
3 0.925 0.200 13 20189241 missense variant T/C snv 1.5E-02 5.1E-03 0.030 1.000 3 2009 2015
dbSNP: rs2274084
rs2274084
6 0.882 0.240 13 20189503 missense variant C/T snv 5.4E-02 2.2E-02 0.020 0.500 2 2005 2009
dbSNP: rs28931593
rs28931593
9 0.776 0.200 13 20189358 missense variant C/T snv 7.0E-06 0.020 1.000 2 2002 2014
dbSNP: rs111033196
rs111033196
2 1.000 0.120 13 20189202 missense variant C/A;T snv 2.8E-04; 1.4E-02 0.010 1.000 1 2010 2010
dbSNP: rs111033293
rs111033293
10 0.763 0.280 13 20189581 start lost T/A;C snv 3.6E-05 4.2E-05 0.010 1.000 1 2014 2014
dbSNP: rs111033361
rs111033361
1 13 20189355 missense variant A/G snv 2.0E-05 7.0E-06 0.010 1.000 1 2009 2009
dbSNP: rs1476034902
rs1476034902
1 13 20189542 missense variant T/C snv 1.4E-05 0.010 1.000 1 2006 2006
dbSNP: rs750795475
rs750795475
1 13 20189144 synonymous variant G/A snv 4.0E-06 7.0E-06 0.010 1.000 1 2002 2002
dbSNP: rs755058488
rs755058488
1 13 20189186 synonymous variant C/T snv 4.0E-06 7.0E-06 0.010 1.000 1 2001 2001
dbSNP: rs774518779
rs774518779
9 0.776 0.280 13 20189076 missense variant C/T snv 8.0E-06 0.010 1.000 1 2014 2014
dbSNP: rs781534323
rs781534323
2 1.000 0.120 13 20189336 missense variant G/C snv 8.0E-06 7.0E-06 0.010 1.000 1 2002 2002