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: rs5000770
rs5000770
3 0.882 0.160 15 80424141 intron variant G/A snv 0.27 0.020 1.000 2 2012 2012
dbSNP: rs1020397
rs1020397
3 0.882 0.160 15 80426396 intron variant G/C;T snv 0.010 1.000 1 2012 2012