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: rs1462891
rs1462891
1 1.000 0.200 8 31973417 intron variant T/C snv 0.72 0.010 1.000 1 2013 2013
dbSNP: rs383632
rs383632
1 1.000 0.200 8 31948532 intron variant T/C;G snv 0.010 1.000 1 2013 2013