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: rs9277535
rs9277535
13 0.724 0.440 6 33087084 3 prime UTR variant A/G snv 0.25 0.710 1.000 3 2007 2018
dbSNP: rs9277554
rs9277554
7 0.790 0.520 6 33087761 3 prime UTR variant C/T snv 0.38 0.700 1.000 3 2007 2011
dbSNP: rs987870
rs987870
4 0.851 0.160 6 33075103 intron variant A/G snv 0.19 0.700 1.000 2 2007 2009
dbSNP: rs1042448
rs1042448
1 1.000 0.120 6 33086565 3 prime UTR variant T/A;C snv 6.1E-03; 7.4E-06 0.700 1.000 1 2011 2011
dbSNP: rs1042544
rs1042544
2 0.925 0.200 6 33086680 3 prime UTR variant A/G snv 0.38 0.700 1.000 1 2011 2011
dbSNP: rs1431403
rs1431403
2 0.925 0.200 6 33079254 intron variant T/C snv 0.37 0.700 1.000 1 2011 2011
dbSNP: rs3091282
rs3091282
2 0.925 0.200 6 33089421 3 prime UTR variant G/C snv 0.38 0.700 1.000 1 2011 2011
dbSNP: rs3091283
rs3091283
1 1.000 0.120 6 33089436 3 prime UTR variant C/T snv 0.33 0.700 1.000 1 2011 2011
dbSNP: rs3091284
rs3091284
1 1.000 0.120 6 33089467 3 prime UTR variant T/G snv 0.32 0.700 1.000 1 2011 2011
dbSNP: rs3097652
rs3097652
2 0.925 0.200 6 33090058 downstream gene variant C/A;T snv 0.700 1.000 1 2011 2011
dbSNP: rs3097674
rs3097674
1 1.000 0.120 6 33082906 intron variant A/C;G snv 0.700 1.000 1 2011 2011
dbSNP: rs3117226
rs3117226
1 1.000 0.120 6 33089882 downstream gene variant G/A snv 0.33 0.700 1.000 1 2011 2011
dbSNP: rs3117228
rs3117228
2 0.925 0.200 6 33088658 3 prime UTR variant G/T snv 0.38 0.700 1.000 1 2011 2011
dbSNP: rs3128960
rs3128960
1 1.000 0.120 6 33082877 intron variant G/A snv 0.38 0.700 1.000 1 2011 2011
dbSNP: rs3128961
rs3128961
2 0.925 0.200 6 33082965 intron variant G/A snv 0.38 0.700 1.000 1 2011 2011
dbSNP: rs3128963
rs3128963
2 0.925 0.200 6 33088003 3 prime UTR variant C/T snv 0.38 0.700 1.000 1 2011 2011
dbSNP: rs3130188
rs3130188
2 0.925 0.200 6 33089399 3 prime UTR variant T/C snv 0.38 0.700 1.000 1 2011 2011
dbSNP: rs9277359
rs9277359
2 0.925 0.200 6 33082247 intron variant C/A;T snv 0.700 1.000 1 2011 2011
dbSNP: rs9277377
rs9277377
1 1.000 0.120 6 33082426 intron variant C/A;G snv 0.700 1.000 1 2011 2011
dbSNP: rs9277378
rs9277378
5 0.827 0.320 6 33082502 intron variant A/G snv 0.40 0.700 1.000 1 2011 2011
dbSNP: rs9277394
rs9277394
2 0.925 0.200 6 33083193 intron variant A/T snv 0.38 0.700 1.000 1 2011 2011
dbSNP: rs9277395
rs9277395
2 0.925 0.200 6 33083274 intron variant A/G snv 0.38 0.700 1.000 1 2011 2011
dbSNP: rs9277396
rs9277396
2 0.925 0.200 6 33083362 intron variant G/A snv 0.38 0.700 1.000 1 2011 2011
dbSNP: rs9277409
rs9277409
2 0.925 0.200 6 33083847 non coding transcript exon variant C/G snv 0.38 0.700 1.000 1 2011 2011
dbSNP: rs9277410
rs9277410
2 0.925 0.200 6 33083863 non coding transcript exon variant G/A snv 0.38 0.700 1.000 1 2011 2011