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: rs3096277
rs3096277
2 16 83730599 intron variant T/C snv 0.74 0.700 1.000 1 2007 2007
dbSNP: rs7069923
rs7069923
2 10 18441439 intron variant C/T snv 0.36 0.700 1.000 1 2009 2009
dbSNP: rs4373814
rs4373814
5 10 18131043 intergenic variant G/C;T snv 0.700 1.000 1 2011 2011
dbSNP: rs6825911
rs6825911
3 4 110460482 intron variant C/T snv 0.68 0.700 1.000 1 2011 2011
dbSNP: rs805303
rs805303
7 0.925 0.160 6 31648589 intron variant G/A snv 0.45 0.700 1.000 1 2011 2011
dbSNP: rs10826334
rs10826334
3 10 59620724 intron variant C/A;G snv 0.700 1.000 1 2013 2013
dbSNP: rs10832417
rs10832417
3 11 2631427 non coding transcript exon variant T/G snv 0.32 0.700 1.000 1 2013 2013
dbSNP: rs10841530
rs10841530
2 12 20446178 intron variant A/G snv 0.30 0.700 1.000 1 2013 2013
dbSNP: rs11693319
rs11693319
2 2 178873542 3 prime UTR variant C/G;T snv 0.700 1.000 1 2013 2013
dbSNP: rs13178964
rs13178964
2 5 105011948 intron variant A/G snv 0.17 0.700 1.000 1 2013 2013
dbSNP: rs1401454
rs1401454
3 11 16228637 intron variant C/A;G;T snv 0.700 1.000 1 2013 2013
dbSNP: rs1669539
rs1669539
2 1.000 0.080 2 105998818 intergenic variant T/C snv 7.1E-02 0.700 1.000 1 2013 2013
dbSNP: rs16890334
rs16890334
3 6 78846449 intergenic variant T/C snv 1.9E-03 0.700 1.000 1 2013 2013
dbSNP: rs16963349
rs16963349
2 16 84304628 intron variant T/C snv 7.4E-02 0.700 1.000 1 2013 2013
dbSNP: rs2410182
rs2410182
2 21 39808149 intergenic variant A/G;T snv 0.700 1.000 1 2013 2013
dbSNP: rs2735413
rs2735413
2 16 78019746 intron variant A/C;T snv 0.700 1.000 1 2013 2013
dbSNP: rs2837253
rs2837253
2 21 39849329 intergenic variant G/A;T snv 0.700 1.000 1 2013 2013
dbSNP: rs4460079
rs4460079
2 4 113940144 intron variant C/T snv 0.58 0.700 1.000 1 2013 2013
dbSNP: rs4494364
rs4494364
2 12 91083337 intergenic variant G/A snv 0.17 0.700 1.000 1 2013 2013
dbSNP: rs648425
rs648425
2 1 78421523 intron variant T/C snv 0.95 0.700 1.000 1 2013 2013
dbSNP: rs7116456
rs7116456
2 11 23933767 intergenic variant T/C snv 0.97 0.700 1.000 1 2013 2013
dbSNP: rs7577262
rs7577262
4 2 233910224 intergenic variant G/A;T snv 0.700 1.000 1 2013 2013
dbSNP: rs7658266
rs7658266
2 4 113942550 intron variant T/A;C snv 0.700 1.000 1 2013 2013
dbSNP: rs7952106
rs7952106
2 1.000 0.080 11 113553836 regulatory region variant G/T snv 0.71 0.700 1.000 1 2013 2013
dbSNP: rs8002688
rs8002688
2 13 72985844 intron variant C/T snv 0.12 0.700 1.000 1 2013 2013