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: rs34002892
rs34002892
8 0.851 0.200 12 101753470 frameshift variant GA/- delins 5.1E-04 3.5E-04 0.700 1.000 3 2006 2014
dbSNP: rs1562927768
rs1562927768
15 0.790 0.080 7 105101476 frameshift variant AAAGA/- delins 0.700 0
dbSNP: rs1562931936
rs1562931936
5 1.000 7 105107527 stop gained C/T snv 0.700 0
dbSNP: rs1557739557
rs1557739557
1 1 11114402 missense variant C/T snv 0.700 0
dbSNP: rs587777893
rs587777893
67 0.658 0.240 1 11128107 missense variant G/A;T snv 0.700 1.000 1 2016 2016
dbSNP: rs121918470
rs121918470
10 0.790 0.160 12 112489105 missense variant A/C;G snv 4.0E-06 0.700 1.000 4 2004 2006
dbSNP: rs1064794254
rs1064794254
6 0.851 0.120 X 119841185 frameshift variant CT/- delins 0.700 1.000 3 2007 2012
dbSNP: rs1565339091
rs1565339091
4 1.000 0.200 11 124924796 missense variant T/C snv 0.700 0
dbSNP: rs1554776954
rs1554776954
5 1.000 9 127661133 frameshift variant A/- delins 0.700 0
dbSNP: rs869312702
rs869312702
10 0.827 0.160 9 128203609 missense variant G/A snv 0.700 0
dbSNP: rs786205861
rs786205861
3 1.000 0.120 19 12896913 missense variant C/T snv 0.700 0
dbSNP: rs782609482
rs782609482
4 1.000 0.120 9 133352060 splice donor variant C/A;T snv 4.1E-06 0.700 0
dbSNP: rs869312669
rs869312669
2 1.000 12 13571922 missense variant T/G snv 0.700 0
dbSNP: rs1564365418
rs1564365418
5 0.882 0.120 9 137163846 missense variant G/T snv 0.700 0
dbSNP: rs397507483
rs397507483
13 0.790 0.400 7 140753348 missense variant C/A;T snv 0.700 0
dbSNP: rs121913355
rs121913355
42 0.641 0.520 7 140781602 missense variant C/A;G;T snv 4.0E-06 0.700 0
dbSNP: rs121913348
rs121913348
20 0.763 0.480 7 140781617 missense variant C/A;G;T snv 0.700 1.000 1 2008 2008
dbSNP: rs180177035
rs180177035
35 0.752 0.280 7 140801502 missense variant T/C snv 0.700 1.000 2 2006 2006
dbSNP: rs1554639173
rs1554639173
3 1.000 9 14120609 frameshift variant TTCGAGTTGAGATG/- delins 0.700 0
dbSNP: rs1554649366
rs1554649366
3 1.000 9 14150191 frameshift variant -/CA delins 0.700 0
dbSNP: rs1554709654
rs1554709654
3 1.000 9 14307156 missense variant A/G snv 0.700 0
dbSNP: rs1554709662
rs1554709662
3 1.000 9 14307175 missense variant T/C snv 0.700 0
dbSNP: rs1554709683
rs1554709683
3 1.000 9 14307210 missense variant T/G snv 0.700 0
dbSNP: rs764333096
rs764333096
3 1.000 9 14307286 stop gained G/A;T snv 2.0E-05 0.700 0
dbSNP: rs1554709792
rs1554709792
3 1.000 9 14307442 stop gained G/A snv 0.700 0