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: rs393795
rs393795
4 0.851 0.160 5 1428399 intron variant G/T snv 0.28 0.020 1.000 2 2010 2010
dbSNP: rs1042098
rs1042098
1 1.000 0.160 5 1394700 3 prime UTR variant A/G snv 0.25 0.31 0.010 < 0.001 1 2010 2010