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: rs10872673
rs10872673
1 6 151534458 intron variant G/T snv 0.45 0.700 1.000 1 2019 2019
dbSNP: rs10882397
rs10882397
2 10 94132902 intron variant C/A snv 0.52 0.700 1.000 1 2019 2019
dbSNP: rs10942863
rs10942863
1 5 78550731 intron variant C/G;T snv 0.39 0.700 1.000 1 2019 2019
dbSNP: rs11017236
rs11017236
1 10 130401217 intron variant T/A snv 0.28 0.700 1.000 1 2008 2008
dbSNP: rs11048457
rs11048457
1 12 26310241 intron variant G/A snv 0.62 0.700 1.000 1 2019 2019
dbSNP: rs11111839
rs11111839
1 12 103916945 intron variant C/A snv 7.9E-02 0.700 1.000 1 2008 2008
dbSNP: rs11130381
rs11130381
1 3 53815978 3 prime UTR variant C/T snv 0.47 0.700 1.000 1 2019 2019
dbSNP: rs11231711
rs11231711
1 11 64161743 intron variant G/A snv 8.1E-02 0.700 1.000 1 2019 2019
dbSNP: rs112684153
rs112684153
1 13 41275595 intergenic variant T/C;G snv 0.700 1.000 1 2019 2019
dbSNP: rs113230003
rs113230003
2 19 18350146 intron variant G/A snv 0.25 0.700 1.000 1 2019 2019
dbSNP: rs113602013
rs113602013
1 18 60252477 intergenic variant G/A;C snv 0.700 1.000 1 2019 2019
dbSNP: rs113898337
rs113898337
1 2 20567381 intron variant C/G snv 4.1E-03 0.700 1.000 1 2019 2019
dbSNP: rs1149643
rs1149643
1 1 56163763 intron variant A/T snv 0.49 0.700 1.000 1 2019 2019
dbSNP: rs115262049
rs115262049
1 2 42969554 regulatory region variant A/T snv 5.6E-02 0.700 1.000 1 2019 2019
dbSNP: rs1154988
rs1154988
7 3 136206349 upstream gene variant T/A snv 0.76 0.700 1.000 1 2019 2019
dbSNP: rs1155311
rs1155311
1 11 83778372 intron variant A/T snv 0.66 0.700 1.000 1 2019 2019
dbSNP: rs11601694
rs11601694
1 11 47593023 intron variant C/A;T snv 0.700 1.000 1 2019 2019
dbSNP: rs11605518
rs11605518
1 11 13248667 intergenic variant A/G snv 0.72 0.700 1.000 1 2019 2019
dbSNP: rs11647570
rs11647570
1 16 4087261 intron variant A/G snv 0.20 0.700 1.000 1 2019 2019
dbSNP: rs11709060
rs11709060
1 3 128075405 intron variant G/A snv 3.1E-02 0.700 1.000 1 2019 2019
dbSNP: rs11724647
rs11724647
1 4 155725188 intron variant T/A;C snv 0.700 1.000 1 2019 2019
dbSNP: rs117539635
rs117539635
2 15 69390577 intron variant A/G snv 1.6E-02 0.700 1.000 1 2019 2019
dbSNP: rs11767188
rs11767188
1 7 27532326 intron variant A/G;T snv 0.700 1.000 1 2019 2019
dbSNP: rs11770148
rs11770148
1 7 1859811 intron variant A/G;T snv 0.700 1.000 1 2019 2019
dbSNP: rs11781816
rs11781816
1 8 142916379 intron variant C/T snv 0.33 0.31 0.700 1.000 1 2019 2019