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: rs1157699
rs1157699
2 0.925 0.040 2 187394177 intron variant C/G;T snv 0.010 1.000 1 2009 2009
dbSNP: rs6759535
rs6759535
2 0.925 0.040 2 187373374 intron variant T/C snv 0.52 0.010 1.000 1 2009 2009
dbSNP: rs840617
rs840617
2 0.925 0.040 2 187365606 intron variant A/T snv 0.80 0.010 1.000 1 2009 2009