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: rs1431401
rs1431401
1 1.000 0.080 6 33073409 intron variant G/A snv 0.29 0.700 1.000 1 2013 2013
dbSNP: rs154972
rs154972
2 0.925 0.120 6 32932874 downstream gene variant A/G snv 0.35 0.700 1.000 1 2011 2011
dbSNP: rs154977
rs154977
1 1.000 0.080 6 32932241 downstream gene variant C/G;T snv 0.700 1.000 1 2013 2013
dbSNP: rs17056316
rs17056316
1 1.000 0.080 4 170892334 downstream gene variant A/G snv 2.6E-03 0.700 1.000 1 2013 2013
dbSNP: rs17214519
rs17214519
1 1.000 0.080 6 33064411 downstream gene variant G/A;T snv 0.700 1.000 1 2013 2013
dbSNP: rs1897824
rs1897824
1 1.000 0.080 19 44472854 non coding transcript exon variant T/A;C snv 0.700 1.000 1 2013 2013
dbSNP: rs204999
rs204999
13 0.763 0.480 6 32142202 intergenic variant A/G snv 0.28 0.700 1.000 1 2011 2011
dbSNP: rs2051549
rs2051549
4 0.851 0.280 6 32762309 intron variant G/A snv 0.64 0.700 1.000 1 2013 2013
dbSNP: rs2051598
rs2051598
1 1.000 0.080 6 32741586 intron variant G/A snv 0.71 0.700 1.000 1 2013 2013
dbSNP: rs2064476
rs2064476
2 0.925 0.200 6 33105545 intron variant A/G snv 0.37 0.700 1.000 1 2013 2013
dbSNP: rs2071351
rs2071351
1 1.000 0.080 6 33076153 intron variant A/G snv 0.24 0.29 0.700 1.000 1 2013 2013
dbSNP: rs2071353
rs2071353
1 1.000 0.080 6 33076480 intron variant T/C;G snv 0.700 1.000 1 2013 2013
dbSNP: rs2071551
rs2071551
1 1.000 0.080 6 32761682 synonymous variant C/G;T snv 0.67 0.700 1.000 1 2013 2013
dbSNP: rs2213565
rs2213565
1 1.000 0.080 6 32745411 splice region variant C/T snv 0.81 0.80 0.700 1.000 1 2013 2013
dbSNP: rs2213573
rs2213573
2 0.925 0.200 6 32748245 downstream gene variant G/A snv 0.80 0.700 1.000 1 2013 2013
dbSNP: rs2243873
rs2243873
3 1.000 0.080 6 31895656 non coding transcript exon variant C/A snv 0.61 0.700 1.000 1 2013 2013
dbSNP: rs2253705
rs2253705
1 1.000 0.080 6 30932317 intron variant T/C snv 0.74 0.700 1.000 1 2013 2013
dbSNP: rs2256609
rs2256609
2 0.925 0.080 22 21570728 intron variant A/G snv 0.18 0.700 1.000 1 2013 2013
dbSNP: rs2266959
rs2266959
9 0.776 0.200 22 21568615 intron variant G/T snv 0.18 0.700 1.000 1 2013 2013
dbSNP: rs2266961
rs2266961
7 0.807 0.160 22 21574308 intron variant C/G snv 0.18 0.700 1.000 1 2013 2013
dbSNP: rs2266963
rs2266963
1 1.000 0.080 22 21593178 intron variant C/G snv 0.18 0.700 1.000 1 2013 2013
dbSNP: rs2295119
rs2295119
2 0.925 0.120 6 33093093 non coding transcript exon variant G/T snv 0.14 0.700 1.000 1 2018 2018
dbSNP: rs2298428
rs2298428
9 0.807 0.240 22 21628603 missense variant C/T snv 0.27 0.18 0.700 1.000 1 2013 2013
dbSNP: rs2301224
rs2301224
1 1.000 0.080 6 33070592 intron variant C/A snv 0.28 0.700 1.000 1 2013 2013
dbSNP: rs2301226
rs2301226
1 1.000 0.080 6 33066819 non coding transcript exon variant G/A snv 0.16 0.700 1.000 1 2011 2011