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: rs1081725
rs1081725
1 1.000 0.040 19 23269280 non coding transcript exon variant G/A snv 0.010 1.000 1 2016 2016
dbSNP: rs111033565
rs111033565
11 0.742 0.120 7 142751938 missense variant G/A snv 1.2E-05 0.010 1.000 1 2008 2008
dbSNP: rs111033566
rs111033566
11 0.742 0.280 7 142750600 missense variant A/C;T snv 0.010 1.000 1 2008 2008
dbSNP: rs121909293
rs121909293
5 0.851 0.080 1 15445717 missense variant C/T snv 4.4E-03 3.8E-03 0.010 1.000 1 2011 2011
dbSNP: rs121913228
rs121913228
14 0.742 0.200 3 41224621 missense variant T/C;G snv 0.010 1.000 1 2007 2007
dbSNP: rs1223231582
rs1223231582
24 0.677 0.280 7 142750639 missense variant A/G snv 7.0E-06 0.010 1.000 1 2008 2008
dbSNP: rs1451011538
rs1451011538
2 0.925 0.080 16 84838647 missense variant T/A snv 4.0E-06 0.010 1.000 1 2008 2008
dbSNP: rs146646971
rs146646971
RET
7 0.807 0.120 10 43114598 missense variant G/C;T snv 2.4E-05 0.010 1.000 1 2016 2016
dbSNP: rs1485866385
rs1485866385
APC
1 1.000 0.040 5 112767287 missense variant T/G snv 1.4E-05 0.010 1.000 1 2007 2007
dbSNP: rs1489694587
rs1489694587
DMD
3 0.882 0.120 X 31172385 missense variant A/C snv 0.010 < 0.001 1 2003 2003
dbSNP: rs1501899
rs1501899
8 0.790 0.240 3 122188481 intron variant A/G snv 0.62 0.010 1.000 1 2015 2015
dbSNP: rs1544410
rs1544410
VDR
78 0.542 0.760 12 47846052 intron variant C/A;G;T snv 0.010 1.000 1 2018 2018
dbSNP: rs202199891
rs202199891
APC
3 0.925 0.080 5 112827969 missense variant T/C snv 3.2E-05 2.1E-05 0.010 1.000 1 2020 2020
dbSNP: rs2073618
rs2073618
19 0.716 0.480 8 118951813 missense variant G/C snv 0.52 0.60 0.010 1.000 1 2011 2011
dbSNP: rs267606982
rs267606982
11 0.742 0.120 7 142751938 missense variant GC/AT mnv 0.010 1.000 1 2008 2008
dbSNP: rs3102735
rs3102735
12 0.752 0.400 8 118952831 upstream gene variant T/C snv 0.17 0.010 < 0.001 1 2011 2011
dbSNP: rs3134070
rs3134070
3 0.882 0.200 8 118952785 upstream gene variant C/T snv 9.6E-02 0.010 < 0.001 1 2011 2011
dbSNP: rs397508687
rs397508687
5 0.827 0.080 7 117531040 frameshift variant -/GA ins 4.0E-06 0.010 1.000 1 2008 2008
dbSNP: rs61734277
rs61734277
5 0.882 0.080 6 10874672 missense variant A/C snv 9.1E-03 8.6E-03 0.010 1.000 1 2014 2014
dbSNP: rs61734659
rs61734659
8 0.790 0.160 7 142774035 missense variant G/A snv 1.4E-02 0.010 1.000 1 2011 2011
dbSNP: rs74799832
rs74799832
RET
33 0.662 0.280 10 43121968 missense variant T/C snv 4.0E-06 0.010 1.000 1 2006 2006
dbSNP: rs748405415
rs748405415
8 0.790 0.160 7 142773993 stop gained G/A;T snv 0.010 1.000 1 2011 2011
dbSNP: rs76371115
rs76371115
6 0.807 0.160 7 117531041 missense variant A/C;G;T snv 8.0E-06 0.010 1.000 1 2008 2008
dbSNP: rs7652589
rs7652589
13 0.732 0.400 3 122170241 downstream gene variant A/G snv 0.60 0.010 1.000 1 2011 2011
dbSNP: rs775437927
rs775437927
3 0.882 0.080 16 84849390 missense variant G/A snv 6.0E-05 7.0E-06 0.010 1.000 1 2008 2008