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: rs10084572
rs10084572
3 1.000 0.040 21 43992991 downstream gene variant T/A;C;G snv 0.700 1.000 1 2019 2019
dbSNP: rs10224002
rs10224002
12 0.925 0.080 7 151717955 intron variant A/G snv 0.31 0.700 1.000 1 2018 2018
dbSNP: rs10224210
rs10224210
9 1.000 0.040 7 151716108 intron variant T/C snv 0.21 0.700 1.000 1 2019 2019
dbSNP: rs10401969
rs10401969
25 0.776 0.240 19 19296909 intron variant T/C snv 0.10 0.700 1.000 1 2016 2016
dbSNP: rs1047891
rs1047891
34 0.827 0.200 2 210675783 missense variant C/A snv 0.30 0.33 0.700 1.000 1 2019 2019
dbSNP: rs10497721
rs10497721
2 1.000 0.040 2 192049636 intron variant C/A;T snv 0.700 1.000 1 2007 2007
dbSNP: rs10811652
rs10811652
4 0.882 0.120 9 22077086 intron variant A/C;T snv 0.700 1.000 1 2018 2018
dbSNP: rs10941191
rs10941191
3 1.000 0.040 5 34504693 intergenic variant C/A;T snv 0.700 1.000 1 2019 2019
dbSNP: rs11124945
rs11124945
3 1.000 0.040 2 43650017 intron variant A/G snv 0.21 0.700 1.000 1 2018 2018
dbSNP: rs113296370
rs113296370
3 1.000 0.040 2 43636315 upstream gene variant A/C snv 0.17 0.700 1.000 1 2018 2018
dbSNP: rs11622435
rs11622435
7 0.827 0.120 14 81151652 intron variant G/A snv 4.7E-02 0.700 1.000 1 2018 2018
dbSNP: rs11864909
rs11864909
7 0.851 0.160 16 20389517 intron variant C/T snv 0.23 0.700 1.000 1 2018 2018
dbSNP: rs12310617
rs12310617
16 0.851 0.120 12 3060327 intergenic variant C/T snv 0.11 0.700 1.000 1 2016 2016
dbSNP: rs12369179
rs12369179
16 0.851 0.120 12 122479003 intron variant C/T snv 5.9E-02 0.700 1.000 1 2016 2016
dbSNP: rs12420422
rs12420422
16 0.851 0.120 11 123009573 intergenic variant G/A snv 3.4E-02 0.700 1.000 1 2016 2016
dbSNP: rs12579302
rs12579302
19 0.851 0.120 12 89656726 intron variant A/G snv 0.15 0.700 1.000 1 2016 2016
dbSNP: rs1264347
rs1264347
4 1.000 0.040 6 30830920 upstream gene variant C/T snv 7.9E-02 0.700 1.000 1 2019 2019
dbSNP: rs12917707
rs12917707
11 0.827 0.200 16 20356368 upstream gene variant G/T snv 0.14 0.700 1.000 1 2016 2016
dbSNP: rs12922822
rs12922822
5 1.000 0.040 16 20356323 upstream gene variant C/A;T snv 0.700 1.000 1 2019 2019
dbSNP: rs13114738
rs13114738
16 0.851 0.120 4 102363708 intron variant C/A;T snv 0.700 1.000 1 2016 2016
dbSNP: rs13146355
rs13146355
6 1.000 0.040 4 76490987 intron variant G/A snv 0.33 0.700 1.000 1 2019 2019
dbSNP: rs13191445
rs13191445
4 0.925 0.120 6 26015261 upstream gene variant G/A snv 5.6E-02 0.700 1.000 1 2019 2019
dbSNP: rs1333048
rs1333048
24 0.683 0.320 9 22125348 intron variant A/C snv 0.44 0.700 1.000 1 2016 2016
dbSNP: rs13427836
rs13427836
2 1.000 0.040 2 128270387 intron variant C/T snv 0.11 0.700 1.000 1 2016 2016
dbSNP: rs145590578
rs145590578
3 1.000 0.040 6 160236104 intron variant GTT/- delins 9.8E-02 0.700 1.000 1 2019 2019