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: rs1153280
rs1153280
2 1.000 0.120 21 29305751 intron variant G/A snv 0.52 0.700 1.000 1 2011 2011
dbSNP: rs1153287
rs1153287
1 1.000 0.120 21 29313290 intron variant G/A;T snv 0.700 1.000 1 2011 2011
dbSNP: rs1153294
rs1153294
1 1.000 0.120 21 29328775 intron variant T/C;G snv 0.700 1.000 1 2011 2011
dbSNP: rs117214
rs117214
1 1.000 0.120 21 29348513 intron variant C/T snv 0.45 0.700 1.000 1 2011 2011
dbSNP: rs2027605
rs2027605
3 1.000 0.120 21 29354452 intron variant A/G snv 0.48 0.700 1.000 1 2011 2011
dbSNP: rs2832290
rs2832290
1 1.000 0.120 21 29356542 intron variant A/G snv 0.48 0.700 1.000 1 2011 2011
dbSNP: rs372883
rs372883
5 0.827 0.360 21 29345416 3 prime UTR variant T/C snv 0.53 0.700 1.000 1 2011 2011