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: rs102275
rs102275
18 0.827 0.320 11 61790331 non coding transcript exon variant T/C snv 0.47 0.800 1.000 3 2011 2013
dbSNP: rs17606561
rs17606561
2 1.000 0.040 6 10982126 3 prime UTR variant G/A snv 0.17 0.800 1.000 2 2011 2012
dbSNP: rs603424
rs603424
13 1.000 0.080 10 100315722 intron variant G/A snv 0.34 0.800 1.000 2 2012 2013
dbSNP: rs780093
rs780093
30 0.763 0.240 2 27519736 intron variant T/C snv 0.68 0.700 1.000 2 2011 2013
dbSNP: rs1000778
rs1000778
3 1.000 0.040 11 61887833 intron variant A/G snv 0.59 0.700 1.000 1 2011 2011
dbSNP: rs1007323
rs1007323
1 6 10953011 intron variant T/A;G snv 0.700 1.000 1 2011 2011
dbSNP: rs10220265
rs10220265
1 13 103397233 downstream gene variant G/A snv 0.28 0.700 1.000 1 2011 2011
dbSNP: rs10237735
rs10237735
2 7 32337136 intron variant C/T snv 7.6E-02 0.700 1.000 1 2013 2013
dbSNP: rs10404486
rs10404486
1 19 52780882 non coding transcript exon variant C/T snv 0.20 0.800 1.000 1 2012 2012
dbSNP: rs10414689
rs10414689
2 19 51293045 regulatory region variant T/C snv 0.11 0.700 1.000 1 2013 2013
dbSNP: rs10468017
rs10468017
12 0.851 0.120 15 58386313 intron variant C/T snv 0.24 0.800 1.000 1 2012 2012
dbSNP: rs10498676
rs10498676
3 0.925 0.040 6 11026766 intron variant G/A snv 0.18 0.700 1.000 1 2011 2011
dbSNP: rs10517480
rs10517480
2 4 59883111 intergenic variant A/T snv 0.27 0.700 1.000 1 2008 2008
dbSNP: rs1058694
rs1058694
1 21 43984239 3 prime UTR variant C/T snv 0.32 0.700 1.000 1 2011 2011
dbSNP: rs1061808
rs1061808
2 6 32168770 3 prime UTR variant T/G snv 0.64 0.800 1.000 1 2012 2012
dbSNP: rs10769780
rs10769780
1 11 7345864 intron variant T/C snv 0.25 0.800 1.000 1 2012 2012
dbSNP: rs1077989
rs1077989
3 1.000 0.080 14 67509105 intron variant A/C snv 0.39 0.800 1.000 1 2012 2012
dbSNP: rs10792320
rs10792320
1 11 61978819 intergenic variant A/C;T snv 0.700 1.000 1 2011 2011
dbSNP: rs10809457
rs10809457
2 9 11402319 intron variant G/T snv 0.36 0.700 1.000 1 2013 2013
dbSNP: rs108499
rs108499
2 11 61779765 intron variant C/T snv 0.27 0.700 1.000 1 2011 2011
dbSNP: rs10885997
rs10885997
2 10 116638460 synonymous variant A/G snv 0.38 0.36 0.800 1.000 1 2012 2012
dbSNP: rs10897208
rs10897208
1 11 62024415 intergenic variant A/T snv 0.11 0.700 1.000 1 2011 2011
dbSNP: rs1109748
rs1109748
2 11 61955173 synonymous variant C/A snv 0.21 0.11 0.700 1.000 1 2011 2011
dbSNP: rs11119805
rs11119805
2 1 211744902 3 prime UTR variant T/A snv 0.13 0.700 1.000 1 2013 2013
dbSNP: rs11120822
rs11120822
2 1 7053052 intron variant G/C snv 0.34 0.700 1.000 1 2013 2013