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: rs2075822
rs2075822
1 1.000 0.040 7 30451144 intron variant A/G snv 0.19 0.010 1.000 1 2006 2006
dbSNP: rs2907748
rs2907748
1 1.000 0.040 7 30433407 non coding transcript exon variant C/T snv 0.20 0.010 1.000 1 2006 2006