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: rs10883371
rs10883371
1 1.000 0.040 10 99532698 upstream gene variant C/A snv 0.54 0.700 1.000 1 2013 2013
dbSNP: rs10905718
rs10905718
1 1.000 0.040 10 6072893 upstream gene variant A/G snv 0.25 0.700 1.000 1 2011 2011
dbSNP: rs11203203
rs11203203
9 0.807 0.240 21 42416077 intron variant G/A snv 0.28 0.700 1.000 1 2013 2013
dbSNP: rs11676348
rs11676348
8 0.790 0.160 2 218145423 regulatory region variant C/G;T snv 0.700 1.000 1 2013 2013
dbSNP: rs12369214
rs12369214
6 0.807 0.120 12 106804833 intron variant G/A snv 0.41 0.700 1.000 1 2013 2013
dbSNP: rs12479056
rs12479056
1 1.000 0.040 2 60948177 synonymous variant T/C snv 0.56 0.62 0.700 1.000 1 2013 2013
dbSNP: rs13132245
rs13132245
1 1.000 0.040 4 122128437 intergenic variant A/G snv 0.11 0.700 1.000 1 2012 2012
dbSNP: rs13140464
rs13140464
2 0.925 0.040 4 122578590 regulatory region variant G/T snv 0.10 0.700 1.000 1 2013 2013
dbSNP: rs17683107
rs17683107
1 1.000 0.040 17 9921085 intron variant G/A snv 0.13 0.700 1.000 1 2011 2011
dbSNP: rs1788097
rs1788097
2 0.925 0.040 18 69876452 intron variant C/T snv 0.56 0.700 1.000 1 2013 2013
dbSNP: rs2836883
rs2836883
4 0.882 0.080 21 39094818 intergenic variant G/A snv 0.23 0.700 1.000 1 2013 2013
dbSNP: rs2844559
rs2844559
1 1.000 0.040 6 31372298 intron variant C/T snv 8.0E-02 0.700 1.000 1 2010 2010
dbSNP: rs3099844
rs3099844
13 0.732 0.400 6 31481199 non coding transcript exon variant C/A snv 0.11 0.700 1.000 1 2010 2010
dbSNP: rs3134883
rs3134883
1 1.000 0.040 10 6058762 intron variant G/A snv 0.23 0.700 1.000 1 2011 2011
dbSNP: rs3184504
rs3184504
92 0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 0.700 1.000 1 2013 2013
dbSNP: rs34762726
rs34762726
BSN
1 1.000 0.040 3 49651777 missense variant G/A snv 0.27 0.28 0.700 1.000 1 2013 2013
dbSNP: rs4147359
rs4147359
2 0.925 0.040 10 6066476 upstream gene variant G/A snv 0.33 0.700 1.000 1 2013 2013
dbSNP: rs415595
rs415595
1 1.000 0.040 16 11269835 intron variant A/G snv 0.46 0.700 1.000 1 2013 2013
dbSNP: rs4391646
rs4391646
1 1.000 0.040 1 166208147 intron variant T/C snv 0.22 0.700 1.000 1 2011 2011
dbSNP: rs56258221
rs56258221
2 0.925 0.040 6 90320722 intron variant T/C snv 0.13 0.700 1.000 1 2013 2013
dbSNP: rs60652743
rs60652743
2 0.925 0.040 19 46702450 intron variant A/G snv 0.16 0.700 1.000 1 2013 2013
dbSNP: rs633683
rs633683
1 1.000 0.040 11 118634025 non coding transcript exon variant T/C snv 0.58 0.700 1.000 1 2013 2013
dbSNP: rs6678400
rs6678400
1 1.000 0.040 1 166208523 intron variant G/T snv 0.22 0.700 1.000 1 2011 2011
dbSNP: rs6720394
rs6720394
2 0.925 0.040 2 111231795 intron variant T/G snv 0.11 0.700 1.000 1 2011 2011
dbSNP: rs694739
rs694739
9 0.763 0.320 11 64329761 upstream gene variant A/G snv 0.28 0.700 1.000 1 2013 2013