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: rs2651899
rs2651899
5 0.882 0.040 1 3167148 intron variant T/A;C snv 0.880 1.000 9 2011 2020
dbSNP: rs10218452
rs10218452
1 1 3159033 intron variant A/G snv 0.23 0.700 1.000 1 2016 2016
dbSNP: rs12135062
rs12135062
1 1 3186748 intron variant G/A;T snv 0.700 1.000 1 2016 2016
dbSNP: rs2075968
rs2075968
1 1 3164677 intron variant C/T snv 0.23 0.700 1.000 1 2016 2016