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: rs2294881
rs2294881
3 1.000 0.040 6 32399827 intron variant T/C snv 0.19 0.700 1.000 1 2013 2013
dbSNP: rs2294882
rs2294882
2 6 32399738 intron variant T/C snv 0.19 0.700 1.000 1 2013 2013
dbSNP: rs2294883
rs2294883
1 6 32399674 intron variant T/A snv 0.19 0.700 1.000 1 2013 2013
dbSNP: rs3763313
rs3763313
7 0.807 0.320 6 32408694 upstream gene variant A/C snv 0.21 0.700 1.000 1 2013 2013
dbSNP: rs4713523
rs4713523
1 6 32398194 intron variant G/A snv 0.19 0.700 1.000 1 2013 2013