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: rs10004195
rs10004195
8 0.790 0.320 4 38783103 upstream gene variant T/A snv 0.29 0.010 1.000 1 2015 2015
dbSNP: rs10022537
rs10022537
2 0.925 0.080 4 16075214 intron variant A/T snv 0.70 0.010 1.000 1 2015 2015
dbSNP: rs10052016
rs10052016
2 0.925 0.080 5 1427996 intron variant A/G snv 0.22 0.010 1.000 1 2013 2013
dbSNP: rs10052657
rs10052657
7 0.807 0.120 5 59111944 intron variant C/A snv 0.17 0.010 1.000 1 2018 2018
dbSNP: rs10088390
rs10088390
2 0.925 0.080 8 41264249 3 prime UTR variant C/G snv 0.19 0.010 1.000 1 2017 2017
dbSNP: rs1011445550
rs1011445550
2 0.925 0.080 17 7676391 missense variant G/C snv 0.010 1.000 1 2011 2011
dbSNP: rs10116253
rs10116253
4 0.851 0.120 9 117702042 upstream gene variant T/C snv 0.28 0.010 1.000 1 2014 2014
dbSNP: rs1016343
rs1016343
8 0.807 0.240 8 127081052 non coding transcript exon variant C/T snv 0.20 0.010 1.000 1 2019 2019
dbSNP: rs1042028
rs1042028
30 0.658 0.440 16 28606193 missense variant C/T snv 0.22 0.30 0.010 1.000 1 2005 2005
dbSNP: rs10421916
rs10421916
2 0.925 0.080 19 17818178 intron variant A/G snv 0.69 0.010 1.000 1 2012 2012
dbSNP: rs1042229
rs1042229
7 0.790 0.280 19 51746419 missense variant A/C;G snv 0.32; 0.13 0.010 1.000 1 2011 2011
dbSNP: rs10434
rs10434
17 0.701 0.480 6 43785475 3 prime UTR variant A/G snv 0.59 0.010 1.000 1 2009 2009
dbSNP: rs1044432
rs1044432
2 0.925 0.080 11 13388251 3 prime UTR variant A/T snv 0.16 0.010 1.000 1 2019 2019
dbSNP: rs1045411
rs1045411
18 0.708 0.360 13 30459095 3 prime UTR variant C/T snv 0.20 0.010 1.000 1 2016 2016
dbSNP: rs10464867
rs10464867
2 0.925 0.080 8 89933370 3 prime UTR variant C/T snv 3.0E-02 0.010 1.000 1 2015 2015
dbSNP: rs10474606
rs10474606
2 0.925 0.080 5 80057163 intron variant G/A snv 0.28 0.010 1.000 1 2016 2016
dbSNP: rs1047840
rs1047840
19 0.708 0.280 1 241878999 missense variant G/A snv 0.36 0.40 0.010 1.000 1 2009 2009
dbSNP: rs1048369
rs1048369
4 0.882 0.160 X 133303309 missense variant G/A snv 0.33 0.38 0.010 1.000 1 2016 2016
dbSNP: rs10484761
rs10484761
7 0.807 0.080 6 40834522 intergenic variant T/C snv 0.31 0.010 1.000 1 2014 2014
dbSNP: rs1050450
rs1050450
43 0.623 0.600 3 49357401 missense variant G/A snv 0.28 0.30 0.010 1.000 1 2016 2016
dbSNP: rs10509670
rs10509670
5 0.851 0.080 10 94308190 intron variant A/G snv 0.30 0.010 1.000 1 2019 2019
dbSNP: rs10511729
rs10511729
11 0.742 0.240 9 23557229 intron variant T/G snv 0.35 0.010 1.000 1 2014 2014
dbSNP: rs1051690
rs1051690
4 0.851 0.080 19 7116952 3 prime UTR variant T/C snv 0.83 0.010 1.000 1 2017 2017
dbSNP: rs1051740
rs1051740
56 0.592 0.760 1 225831932 missense variant T/C snv 0.32 0.27 0.010 1.000 1 2006 2006
dbSNP: rs1053023
rs1053023
4 0.882 0.120 17 42313598 3 prime UTR variant T/A;C snv 0.010 1.000 1 2018 2018