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: rs1014290
rs1014290
6 0.827 0.280 4 10000237 intron variant G/A snv 0.72 0.010 1.000 1 2010 2010
dbSNP: rs6449213
rs6449213
7 0.827 0.240 4 9992591 intron variant C/T snv 0.82 0.010 1.000 1 2010 2010
dbSNP: rs733175
rs733175
5 0.851 0.240 4 10048517 intron variant C/T snv 0.77 0.010 1.000 1 2010 2010
dbSNP: rs737267
rs737267
7 0.851 0.240 4 9933120 intron variant G/A;T snv 0.010 1.000 1 2010 2010