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: rs4336470
rs4336470
1 1.000 0.040 6 104732910 intron variant C/T snv 0.45 0.800 1.000 1 2012 2012
dbSNP: rs2499663
rs2499663
1 1.000 0.040 6 104852695 intron variant C/T snv 0.43 0.700 1.000 1 2012 2012
dbSNP: rs4079063
rs4079063
1 1.000 0.040 6 104818243 intron variant A/G;T snv 0.700 1.000 1 2012 2012
dbSNP: rs9404576
rs9404576
3 0.882 0.160 6 104736765 intron variant T/A;G snv 0.700 1.000 1 2012 2012