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: rs1149222
rs1149222
1 1.000 0.080 7 87444459 intron variant G/T snv 0.67 0.010 1.000 1 2008 2008
dbSNP: rs31672
rs31672
1 1.000 0.080 7 87430383 intron variant C/T snv 0.67 0.010 1.000 1 2008 2008