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: rs1422698
rs1422698
1 5 75147307 missense variant C/G;T snv 0.44 0.700 1.000 1 2009 2009
dbSNP: rs2035191
rs2035191
1 5 75117888 intron variant T/C snv 0.20 0.700 1.000 1 2009 2009
dbSNP: rs3923323
rs3923323
1 5 75076316 intron variant T/C snv 0.14 0.700 1.000 1 2009 2009
dbSNP: rs4345300
rs4345300
1 5 75080746 intron variant C/T snv 0.51 0.700 1.000 1 2009 2009
dbSNP: rs6866661
rs6866661
1 5 75238547 upstream gene variant A/G snv 0.52 0.700 1.000 1 2009 2009