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: rs6939340
rs6939340
4 0.851 0.160 6 22139775 intron variant A/G snv 0.62 0.040 1.000 4 2008 2017
dbSNP: rs4712653
rs4712653
3 0.882 0.080 6 22125735 intron variant T/C;G snv 0.030 1.000 3 2016 2017
dbSNP: rs9295536
rs9295536
3 0.882 0.080 6 22131700 intron variant C/A snv 0.58 0.030 1.000 3 2016 2017