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: rs2277438
rs2277438
5 0.827 0.160 13 42581032 intron variant G/A;C snv 0.030 0.333 3 2010 2019
dbSNP: rs7984870
rs7984870
2 0.925 0.160 13 42572346 intron variant G/C snv 0.46 0.020 0.500 2 2010 2013
dbSNP: rs9533156
rs9533156
8 0.807 0.280 13 42573535 intron variant T/C snv 0.47 0.010 1.000 1 2010 2010