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: rs1250550
rs1250550
5 0.851 0.240 10 79300560 intron variant C/A snv 0.27 0.810 1.000 2 2009 2017
dbSNP: rs1250546
rs1250546
3 0.925 0.080 10 79272775 intron variant A/G snv 0.36 0.800 1.000 1 2012 2012
dbSNP: rs1250566
rs1250566
1 10 79286696 intron variant G/A snv 0.24 0.700 1.000 1 2015 2015