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 0.100 1.000 11 2009 2019
dbSNP: rs7089424
rs7089424
10 0.752 0.200 10 61992400 intron variant T/G snv 0.32 0.090 1.000 9 2009 2019
dbSNP: rs10994982
rs10994982
7 0.790 0.120 10 61950345 intron variant A/G snv 0.49 0.070 0.857 7 2009 2019
dbSNP: rs10740055
rs10740055
7 0.790 0.240 10 61958720 intron variant C/A snv 0.49 0.020 1.000 2 2010 2014
dbSNP: rs7073837
rs7073837
4 0.851 0.120 10 61940136 intron variant A/C snv 0.58 0.64 0.020 1.000 2 2010 2014
dbSNP: rs10821938
rs10821938
2 0.925 0.120 10 61965014 intron variant A/C snv 0.56 0.010 1.000 1 2010 2010