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: rs10821936
rs10821936
11 0.742 0.200 10 61963818 intron variant C/T snv 0.69 0.810 1.000 5 2009 2019
dbSNP: rs7089424
rs7089424
10 0.752 0.200 10 61992400 intron variant T/G snv 0.32 0.800 1.000 2 2009 2018
dbSNP: rs10994982
rs10994982
7 0.790 0.120 10 61950345 intron variant A/G snv 0.49 0.710 1.000 3 2009 2019
dbSNP: rs7896246
rs7896246
2 0.925 0.120 10 61964631 intron variant A/G snv 0.74 0.710 1.000 2 2013 2017
dbSNP: rs10821938
rs10821938
2 0.925 0.120 10 61965014 intron variant A/C snv 0.56 0.700 1.000 1 2013 2013
dbSNP: rs4245595
rs4245595
1 1.000 0.120 10 61963136 intron variant C/T snv 0.69 0.700 1.000 1 2014 2014
dbSNP: rs7073837
rs7073837
4 0.851 0.120 10 61940136 intron variant A/C snv 0.58 0.64 0.700 1.000 1 2013 2013
dbSNP: rs7087125
rs7087125
1 1.000 0.120 10 62013280 intron variant C/T snv 0.37 0.700 1.000 1 2013 2013
dbSNP: rs7923074
rs7923074
1 1.000 0.120 10 61963681 intron variant A/C snv 0.56 0.700 1.000 1 2013 2013
dbSNP: rs10740055
rs10740055
7 0.790 0.240 10 61958720 intron variant C/A snv 0.49 0.010 1.000 1 2017 2017
dbSNP: rs6479778
rs6479778
5 0.827 0.200 10 61929318 intron variant T/C;G snv 0.010 1.000 1 2017 2017