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: rs10520163
rs10520163
2 1.000 0.040 4 169705401 intron variant T/A;C snv 0.700 1.000 1 2017 2017
dbSNP: rs10791097
rs10791097
2 1.000 0.040 11 130848735 intron variant T/G snv 0.60 0.700 1.000 1 2017 2017
dbSNP: rs10791111
rs10791111
2 1.000 0.040 11 130986204 intergenic variant T/G snv 0.45 0.700 1.000 1 2017 2017
dbSNP: rs1080500
rs1080500
2 1.000 0.040 3 53141001 intergenic variant G/A snv 0.27 0.700 1.000 1 2017 2017
dbSNP: rs111312615
rs111312615
2 1.000 0.040 6 29955302 upstream gene variant T/G snv 0.700 1.000 1 2017 2017
dbSNP: rs111639056
rs111639056
2 1.000 0.040 6 32570699 intergenic variant G/A snv 0.12 0.700 1.000 1 2017 2017
dbSNP: rs11191419
rs11191419
2 1.000 0.040 10 102852578 intron variant T/A snv 0.36 0.700 1.000 1 2017 2017
dbSNP: rs11191582
rs11191582
2 1.000 0.040 10 103153896 intron variant G/A snv 7.7E-02 0.700 1.000 1 2017 2017
dbSNP: rs111977918
rs111977918
2 1.000 0.040 6 31268274 downstream gene variant G/A;C snv 0.700 1.000 1 2017 2017
dbSNP: rs11210195
rs11210195
2 1.000 0.040 1 73283600 intergenic variant C/T snv 0.44 0.700 1.000 1 2017 2017
dbSNP: rs112209031
rs112209031
2 1.000 0.040 6 32524630 intron variant T/C;G snv 0.700 1.000 1 2017 2017
dbSNP: rs11223651
rs11223651
2 1.000 0.040 11 133971139 intergenic variant C/T snv 0.16 0.700 1.000 1 2017 2017
dbSNP: rs1131275
rs1131275
2 1.000 0.040 6 31356183 missense variant G/A;C snv 0.68 0.700 1.000 1 2017 2017
dbSNP: rs113205291
rs113205291
2 1.000 0.040 6 29894844 upstream gene variant A/G;T snv 0.700 1.000 1 2017 2017
dbSNP: rs113397282
rs113397282
2 1.000 0.040 6 32520273 intron variant T/C;G snv 0.700 1.000 1 2017 2017
dbSNP: rs114041423
rs114041423
2 1.000 0.040 6 29639270 upstream gene variant G/A snv 0.700 1.000 1 2017 2017
dbSNP: rs114086406
rs114086406
2 1.000 0.040 6 32374760 intron variant G/A snv 0.700 1.000 1 2017 2017
dbSNP: rs114115252
rs114115252
2 1.000 0.040 6 30931418 3 prime UTR variant G/A;C;T snv 0.700 1.000 1 2017 2017
dbSNP: rs114142645
rs114142645
2 1.000 0.040 6 31245806 regulatory region variant T/C snv 0.700 1.000 1 2017 2017
dbSNP: rs114204022
rs114204022
2 1.000 0.040 6 29972902 upstream gene variant G/A snv 0.700 1.000 1 2017 2017
dbSNP: rs114274203
rs114274203
2 1.000 0.040 6 31300843 intron variant C/T snv 0.700 1.000 1 2017 2017
dbSNP: rs114276265
rs114276265
2 1.000 0.040 6 31219298 upstream gene variant C/T snv 0.700 1.000 1 2017 2017
dbSNP: rs114277634
rs114277634
2 1.000 0.040 6 31474954 intron variant T/A;C snv 0.700 1.000 1 2017 2017
dbSNP: rs114291394
rs114291394
2 1.000 0.040 6 31383745 upstream gene variant A/C snv 0.700 1.000 1 2017 2017
dbSNP: rs114441450
rs114441450
2 1.000 0.040 6 30719037 upstream gene variant G/A;T snv 0.700 1.000 1 2017 2017