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: rs587782798
rs587782798
7 0.807 0.400 16 68813322 stop gained C/T snv 0.700 0
dbSNP: rs876658932
rs876658932
7 0.807 0.400 16 68801726 stop gained C/G;T snv 0.700 0
dbSNP: rs10431923
rs10431923
2 0.925 0.120 16 68805360 intron variant G/T snv 0.44 0.010 1.000 1 2018 2018
dbSNP: rs10431924
rs10431924
3 0.882 0.120 16 68805399 intron variant T/C snv 0.45 0.010 1.000 1 2018 2018
dbSNP: rs12185157
rs12185157
3 0.882 0.120 16 68750684 intron variant G/A;C;T snv 0.010 1.000 1 2018 2018
dbSNP: rs13689
rs13689
4 0.851 0.120 16 68834619 3 prime UTR variant T/A;C;G snv 0.010 1.000 1 2018 2018
dbSNP: rs17715799
rs17715799
3 0.882 0.120 16 68796608 intron variant A/G;T snv 0.010 1.000 1 2018 2018
dbSNP: rs4783689
rs4783689
2 0.925 0.080 16 68819768 intron variant C/T snv 0.30 0.010 1.000 1 2018 2018
dbSNP: rs6499199
rs6499199
1 1.000 0.080 16 68815934 intron variant C/T snv 0.14 0.010 1.000 1 2018 2018