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: rs10757275
rs10757275
1 1.000 0.040 9 22106226 intron variant G/A;T snv 0.700 1.000 1 2013 2013
dbSNP: rs10217586
rs10217586
2 1.000 0.040 9 22121350 intron variant A/T snv 0.52 0.700 1.000 1 2013 2013
dbSNP: rs10738606
rs10738606
2 1.000 0.040 9 22088091 intron variant A/T snv 0.42 0.010 1.000 1 2019 2019
dbSNP: rs10757277
rs10757277
2 1.000 0.040 9 22124451 intron variant A/G snv 0.40 0.700 1.000 1 2013 2013
dbSNP: rs1537376
rs1537376
2 1.000 0.040 9 22116221 intron variant T/C snv 0.49 0.700 1.000 1 2013 2013
dbSNP: rs10738609
rs10738609
3 1.000 0.040 9 22114496 intron variant A/C;G;T snv 0.700 1.000 1 2013 2013
dbSNP: rs10757279
rs10757279
3 0.925 0.040 9 22124631 intron variant A/G snv 0.40 0.700 1.000 1 2013 2013
dbSNP: rs2383205
rs2383205
3 0.925 0.080 9 22060936 intron variant A/C;G snv 0.010 1.000 1 2019 2019
dbSNP: rs1333046
rs1333046
4 0.925 0.080 9 22124124 intron variant T/A snv 0.43 0.700 1.000 1 2013 2013
dbSNP: rs944797
rs944797
5 0.882 0.120 9 22115287 intron variant T/C;G snv 0.49 0.800 1.000 3 2011 2013
dbSNP: rs10738610
rs10738610
5 0.882 0.120 9 22123767 intron variant A/C;T snv 0.700 1.000 1 2013 2013
dbSNP: rs2891168
rs2891168
5 0.851 0.160 9 22098620 intron variant A/G snv 0.40 0.700 1.000 1 2013 2013
dbSNP: rs6475606
rs6475606
5 0.882 0.080 9 22081851 intron variant C/T snv 0.62 0.700 1.000 1 2011 2011
dbSNP: rs10757272
rs10757272
6 0.851 0.160 9 22088261 intron variant C/T snv 0.41 0.700 1.000 1 2013 2013
dbSNP: rs1333042
rs1333042
7 0.827 0.120 9 22103814 intron variant A/G snv 0.63 0.820 1.000 5 2011 2016
dbSNP: rs10811656
rs10811656
7 0.807 0.200 9 22124473 intron variant C/T snv 0.47 0.010 1.000 1 2016 2016
dbSNP: rs10116277
rs10116277
8 0.827 0.160 9 22081398 intron variant G/T snv 0.62 0.010 1.000 1 2011 2011
dbSNP: rs7865618
rs7865618
11 0.776 0.240 9 22031006 non coding transcript exon variant G/A;T snv 0.820 1.000 3 2011 2017
dbSNP: rs1333045
rs1333045
14 0.776 0.280 9 22119196 non coding transcript exon variant T/C snv 0.50 0.700 1.000 1 2013 2013
dbSNP: rs1537372
rs1537372
14 0.752 0.120 9 22103184 intron variant G/A;T snv 0.700 1.000 1 2013 2013
dbSNP: rs1333040
rs1333040
15 0.732 0.280 9 22083405 intron variant C/G;T snv 0.030 1.000 3 2011 2016
dbSNP: rs2383206
rs2383206
17 0.742 0.320 9 22115027 intron variant A/G snv 0.49 0.720 1.000 3 2008 2013
dbSNP: rs564398
rs564398
18 0.716 0.360 9 22029548 3 prime UTR variant T/C snv 0.31 0.28 0.800 1.000 2 2011 2018
dbSNP: rs10757274
rs10757274
22 0.701 0.320 9 22096056 intron variant A/G snv 0.41 0.900 1.000 11 2008 2016
dbSNP: rs2383207
rs2383207
22 0.695 0.280 9 22115960 intron variant A/G snv 0.64 0.040 1.000 4 2008 2018