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: rs62309628
rs62309628
1 4 73014333 intergenic variant G/C snv 0.10 0.700 1.000 1 2019 2019
dbSNP: rs17366568
rs17366568
6 0.851 0.200 3 186852664 non coding transcript exon variant G/A snv 8.8E-02 0.800 1.000 2 2010 2017
dbSNP: rs900400
rs900400
7 0.925 0.080 3 157080986 upstream gene variant T/C snv 0.36 0.700 1.000 1 2017 2017
dbSNP: rs4783244
rs4783244
3 0.925 0.120 16 82628663 intron variant G/T snv 0.38 0.800 1.000 3 2011 2014
dbSNP: rs2925979
rs2925979
10 1.000 0.080 16 81501185 intron variant T/A;C snv 0.800 1.000 2 2012 2014
dbSNP: rs10937273
rs10937273
4 0.882 0.160 3 186831906 downstream gene variant G/A snv 0.33 0.800 1.000 1 2014 2014
dbSNP: rs11168618
rs11168618
1 12 48539450 intergenic variant C/T snv 0.33 0.800 1.000 1 2014 2014
dbSNP: rs1187415
rs1187415
1 12 124006982 intron variant G/C snv 0.60 0.800 1.000 1 2014 2014
dbSNP: rs266719
rs266719
1 3 186783859 non coding transcript exon variant T/C snv 0.84 0.800 1.000 1 2014 2014
dbSNP: rs3943077
rs3943077
1 10 121185572 non coding transcript exon variant A/G snv 0.59 0.800 1.000 1 2014 2014
dbSNP: rs889140
rs889140
1 19 33398094 intron variant G/A;C snv 0.800 1.000 1 2014 2014
dbSNP: rs12051272
rs12051272
3 0.925 0.120 16 82629683 intron variant G/C;T snv 0.800 1.000 2 2012 2012
dbSNP: rs10794657
rs10794657
1 1 24299684 intergenic variant A/G snv 0.75 0.800 1.000 1 2012 2012
dbSNP: rs1108842
rs1108842
2 3 52686064 5 prime UTR variant A/C;G;T snv 0.49; 4.0E-06 0.800 1.000 1 2012 2012
dbSNP: rs1515110
rs1515110
1 2 226257500 intergenic variant G/A;C;T snv 0.800 1.000 1 2012 2012
dbSNP: rs182052
rs182052
19 0.701 0.440 3 186842993 intron variant G/A snv 0.38 0.800 1.000 1 2012 2012
dbSNP: rs2590838
rs2590838
3 3 52588070 intron variant G/A snv 0.55 0.800 1.000 1 2012 2012
dbSNP: rs2791553
rs2791553
1 1 219502700 intergenic variant A/G snv 0.57 0.800 1.000 1 2012 2012
dbSNP: rs2980879
rs2980879
3 0.925 0.120 8 125469233 intron variant A/T snv 0.69 0.800 1.000 1 2012 2012
dbSNP: rs3001032
rs3001032
1 1 219554437 upstream gene variant T/C snv 0.35 0.800 1.000 1 2012 2012
dbSNP: rs4301033
rs4301033
1 3 150324831 regulatory region variant G/A snv 0.12 0.800 1.000 1 2012 2012
dbSNP: rs4805885
rs4805885
1 19 33415217 intron variant T/C snv 0.59 0.800 1.000 1 2012 2012
dbSNP: rs592423
rs592423
6 6 139519556 intron variant A/C snv 0.50 0.800 1.000 1 2012 2012
dbSNP: rs6450176
rs6450176
4 5 54002195 intron variant G/A snv 0.27 0.800 1.000 1 2012 2012
dbSNP: rs6488898
rs6488898
1 12 123719285 intron variant G/A snv 0.95 0.800 1.000 1 2012 2012