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: rs4939827
rs4939827
25 0.708 0.160 18 48927093 intron variant T/A;C snv 0.700 1.000 8 2007 2019
dbSNP: rs3184504
rs3184504
92 0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 0.700 1.000 4 2015 2019
dbSNP: rs6066825
rs6066825
10 0.776 0.080 20 48723580 intron variant A/G;T snv 0.700 1.000 4 2015 2019
dbSNP: rs1078643
rs1078643
10 0.776 0.080 17 10803924 missense variant G/A;C snv 0.700 1.000 3 2019 2019
dbSNP: rs6469656
rs6469656
9 0.790 0.080 8 116635549 regulatory region variant G/A;C snv 0.700 1.000 3 2014 2019
dbSNP: rs113488022
rs113488022
490 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 0.020 1.000 2 2013 2018
dbSNP: rs121913377
rs121913377
480 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 0.020 1.000 2 2013 2018
dbSNP: rs12412391
rs12412391
9 0.790 0.080 10 99529178 intron variant A/G;T snv 0.700 1.000 2 2014 2016
dbSNP: rs35107139
rs35107139
11 0.776 0.080 14 53952388 intron variant A/C;G;T snv 0.700 1.000 2 2019 2019
dbSNP: rs45597035
rs45597035
10 0.776 0.080 13 73075014 intron variant A/G;T snv 0.700 1.000 2 2019 2019
dbSNP: rs7226855
rs7226855
9 0.790 0.080 18 48927678 intron variant A/G;T snv 0.700 1.000 2 2015 2019
dbSNP: rs10152518
rs10152518
9 0.790 0.080 15 67884824 intergenic variant G/A;T snv 0.700 1.000 1 2019 2019
dbSNP: rs1057941
rs1057941
18 0.701 0.280 1 155216951 non coding transcript exon variant G/A;T snv 0.46 0.700 1.000 1 2016 2016
dbSNP: rs10951878
rs10951878
9 0.790 0.080 7 46887097 downstream gene variant C/A;T snv 0.700 1.000 1 2019 2019
dbSNP: rs11150038
rs11150038
10 0.790 0.080 16 78042662 intron variant A/C;G snv 0.700 1.000 1 2015 2015
dbSNP: rs11168936
rs11168936
17 0.708 0.280 12 49251457 intron variant T/A;C snv 0.700 1.000 1 2016 2016
dbSNP: rs11196170
rs11196170
10 0.776 0.080 10 112962862 intron variant G/A;C snv 0.700 1.000 1 2019 2019
dbSNP: rs115392158
rs115392158
17 0.708 0.280 6 31347004 intron variant A/G snv 0.700 1.000 1 2016 2016
dbSNP: rs115707823
rs115707823
19 0.701 0.320 6 30374976 intergenic variant G/A snv 0.700 1.000 1 2016 2016
dbSNP: rs11610543
rs11610543
10 0.776 0.080 12 42740389 intergenic variant A/G;T snv 0.700 1.000 1 2019 2019
dbSNP: rs11907546
rs11907546
17 0.708 0.280 20 34131991 upstream gene variant C/A;T snv 0.700 1.000 1 2016 2016
dbSNP: rs1222213359
rs1222213359
62 0.574 0.720 6 43770966 missense variant G/A snv 0.010 1.000 1 2004 2004
dbSNP: rs12255141
rs12255141
9 0.790 0.080 10 112535133 intron variant A/G;T snv 0.700 1.000 1 2019 2019
dbSNP: rs1254244346
rs1254244346
1 1.000 0.080 9 104822502 missense variant G/A snv 4.0E-06 0.010 1.000 1 2016 2016
dbSNP: rs12601991
rs12601991
17 0.708 0.280 17 37741642 intron variant T/A;G snv 0.700 1.000 1 2016 2016