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: rs7574070
rs7574070
1 1.000 0.200 2 191145762 intron variant A/C snv 0.55 0.810 1.000 3 2012 2015
dbSNP: rs7572482
rs7572482
1 1.000 0.200 2 191150346 intron variant A/C;G snv 0.800 1.000 1 2012 2012
dbSNP: rs897200
rs897200
4 0.851 0.280 2 191153045 upstream gene variant T/C snv 0.54 0.800 1.000 1 2012 2012
dbSNP: rs7574865
rs7574865
59 0.574 0.720 2 191099907 intron variant T/G snv 0.79 0.010 1.000 1 2010 2010