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: rs181362
rs181362
3 22 21577779 intron variant C/T snv 0.31 0.800 1.000 4 2010 2019
dbSNP: rs7445
rs7445
2 22 21622758 3 prime UTR variant C/G;T snv 0.22 0.700 1.000 2 2018 2019
dbSNP: rs181360
rs181360
1 22 21574627 intron variant T/G snv 0.21 0.700 1.000 1 2017 2017
dbSNP: rs4821116
rs4821116
3 0.925 0.120 22 21619030 intron variant C/A;T snv 0.18 0.700 1.000 1 2017 2017
dbSNP: rs5754166
rs5754166
3 0.925 0.160 22 21576488 intron variant C/T snv 0.18 0.700 1.000 1 2019 2019
dbSNP: rs5754344
rs5754344
2 1.000 0.080 22 21609497 intron variant A/G snv 0.18 0.700 1.000 1 2015 2015
dbSNP: rs7444
rs7444
2 1.000 0.080 22 21622645 3 prime UTR variant T/C snv 0.32 0.700 1.000 1 2018 2018