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: rs11696652
rs11696652
2 20 35049257 intron variant T/G snv 0.19 0.700 1.000 1 2010 2010
dbSNP: rs11696967
rs11696967
2 20 35155806 intergenic variant A/C snv 0.23 0.700 1.000 1 2010 2010
dbSNP: rs11699306
rs11699306
2 20 35213480 intron variant T/C snv 0.10 0.700 1.000 1 2010 2010
dbSNP: rs11700080
rs11700080
2 20 34458956 intron variant A/C;G snv 0.700 1.000 1 2010 2010
dbSNP: rs11890243
rs11890243
2 2 127200465 intron variant C/A;G snv 0.74 0.700 1.000 1 2010 2010
dbSNP: rs11906318
rs11906318
2 20 35141639 intron variant A/C;T snv 0.700 1.000 1 2010 2010
dbSNP: rs11907010
rs11907010
2 20 35149858 upstream gene variant C/T snv 8.8E-02 0.700 1.000 1 2010 2010
dbSNP: rs11907022
rs11907022
2 20 35695704 intron variant A/G snv 0.10 0.700 1.000 1 2010 2010
dbSNP: rs11908470
rs11908470
2 20 35957141 intron variant A/G snv 8.2E-02 0.700 1.000 1 2010 2010
dbSNP: rs11908683
rs11908683
2 20 35133117 intron variant T/C snv 9.1E-02 0.700 1.000 1 2010 2010
dbSNP: rs1205349
rs1205349
2 20 34311868 upstream gene variant G/C snv 0.72 0.700 1.000 1 2010 2010
dbSNP: rs1205350
rs1205350
2 20 34310533 intron variant G/A snv 0.76 0.700 1.000 1 2010 2010
dbSNP: rs1205357
rs1205357
2 20 34289960 intron variant C/T snv 0.70 0.700 1.000 1 2010 2010
dbSNP: rs12465955
rs12465955
2 2 127249498 non coding transcript exon variant A/G;T snv 0.700 1.000 1 2010 2010
dbSNP: rs12468304
rs12468304
2 2 127436236 3 prime UTR variant C/T snv 0.43 0.700 1.000 1 2010 2010
dbSNP: rs12477670
rs12477670
2 2 127576951 intron variant A/C;G snv 0.700 1.000 1 2010 2010
dbSNP: rs12479003
rs12479003
2 2 127360977 intron variant C/T snv 0.35 0.700 1.000 1 2010 2010
dbSNP: rs12479765
rs12479765
2 20 35237575 intron variant G/A snv 0.17 0.700 1.000 1 2010 2010
dbSNP: rs12480555
rs12480555
2 20 34196688 intron variant A/G snv 0.11 0.700 1.000 1 2010 2010
dbSNP: rs12621149
rs12621149
2 2 127509268 intron variant A/C snv 0.68 0.700 1.000 1 2010 2010
dbSNP: rs12622436
rs12622436
2 2 127324106 intron variant C/A;T snv 0.700 1.000 1 2010 2010
dbSNP: rs12624640
rs12624640
2 20 34364319 intron variant G/A snv 0.31 0.700 1.000 1 2010 2010
dbSNP: rs12625191
rs12625191
2 20 35623371 downstream gene variant C/G snv 6.7E-02 0.700 1.000 1 2010 2010
dbSNP: rs12625272
rs12625272
2 20 34206355 intron variant C/A;G;T snv 0.700 1.000 1 2010 2010
dbSNP: rs13029237
rs13029237
2 2 127390278 intron variant C/T snv 0.34 0.700 1.000 1 2010 2010