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: rs12529
rs12529
10 0.776 0.280 10 5094459 missense variant C/G snv 0.50 0.45 0.010 < 0.001 1 2015 2015
dbSNP: rs1937845
rs1937845
1 1.000 0.120 10 5093956 intron variant A/G snv 0.45 0.010 1.000 1 2015 2015
dbSNP: rs3763676
rs3763676
1 1.000 0.120 10 5094307 intron variant A/G snv 0.35 0.010 1.000 1 2010 2010