Source: ALL
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: rs10005233
rs10005233
1 1.000 0.040 4 89822180 3 prime UTR variant C/T snv 0.58 0.59 0.700 1.000 1 2018 2018
dbSNP: rs10034259
rs10034259
1 1.000 0.040 4 104012596 intron variant A/C snv 0.19 0.700 1.000 1 2018 2018
dbSNP: rs1017730
rs1017730
1 1.000 0.040 11 47711942 intron variant G/A snv 0.18 0.700 1.000 1 2018 2018
dbSNP: rs10501320
rs10501320
5 0.925 0.120 11 47272248 5 prime UTR variant G/C snv 0.17 0.700 1.000 1 2018 2018
dbSNP: rs10507274
rs10507274
2 1.000 0.040 12 116723171 missense variant T/C snv 4.7E-02 4.4E-02 0.700 1.000 1 2018 2018
dbSNP: rs10769256
rs10769256
1 1.000 0.040 11 47356845 intron variant C/G;T snv 0.700 1.000 1 2018 2018
dbSNP: rs10850379
rs10850379
1 1.000 0.040 12 109564972 non coding transcript exon variant C/T snv 0.40 0.700 1.000 1 2018 2018
dbSNP: rs10871777
rs10871777
6 0.925 0.120 18 60184530 intergenic variant A/G snv 0.24 0.700 1.000 1 2018 2018
dbSNP: rs11090045
rs11090045
2 1.000 0.040 22 41357599 3 prime UTR variant G/A;C snv 0.700 1.000 1 2018 2018
dbSNP: rs11159097
rs11159097
1 1.000 0.040 14 74633180 intergenic variant T/A;C snv 0.700 1.000 1 2018 2018
dbSNP: rs11191392
rs11191392
1 1.000 0.040 10 102767194 intron variant C/A snv 0.49 0.700 1.000 1 2018 2018
dbSNP: rs11204421
rs11204421
1 1.000 0.040 17 19994492 intergenic variant T/C snv 0.44 0.700 1.000 1 2018 2018
dbSNP: rs112591851
rs112591851
1 1.000 0.040 19 51749131 intron variant C/T snv 2.1E-02 0.700 1.000 1 2018 2018
dbSNP: rs1163085
rs1163085
INA
1 1.000 0.040 10 103279484 intron variant G/A snv 0.64 0.700 1.000 1 2018 2018
dbSNP: rs11663050
rs11663050
1 1.000 0.040 18 37621190 intron variant T/G snv 0.51 0.700 1.000 1 2018 2018
dbSNP: rs12145083
rs12145083
1 1.000 0.040 1 197853864 intergenic variant T/A snv 0.17 0.700 1.000 1 2018 2018
dbSNP: rs12188167
rs12188167
1 1.000 0.040 5 88370488 intron variant C/G snv 0.15 0.700 1.000 1 2018 2018
dbSNP: rs12260436
rs12260436
1 1.000 0.040 10 102981357 intron variant A/C snv 0.29 0.700 1.000 1 2018 2018
dbSNP: rs12484971
rs12484971
1 1.000 0.040 22 41043300 upstream gene variant A/T snv 0.25 0.700 1.000 1 2018 2018
dbSNP: rs1248860
rs1248860
2 1.000 0.040 3 84966628 intron variant G/A snv 0.56 0.700 1.000 1 2018 2018
dbSNP: rs12765002
rs12765002
2 1.000 0.040 10 102875591 intron variant C/T snv 0.24 0.700 1.000 1 2018 2018
dbSNP: rs12923795
rs12923795
1 1.000 0.040 16 7612705 intron variant A/C;G snv 0.700 1.000 1 2018 2018
dbSNP: rs12938031
rs12938031
6 0.851 0.160 17 45777136 intron variant A/G snv 0.26 0.700 1.000 1 2018 2018
dbSNP: rs12957516
rs12957516
1 1.000 0.040 18 37635554 intron variant C/T snv 0.54 0.700 1.000 1 2018 2018
dbSNP: rs1296171
rs1296171
1 1.000 0.040 1 226871905 intron variant C/A;G snv 0.700 1.000 1 2018 2018