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: rs524952
rs524952
6 0.827 0.040 15 34713685 intergenic variant T/A snv 0.50 0.710 1.000 3 2010 2014
dbSNP: rs2969180
rs2969180
2 1.000 17 11504584 intron variant G/A snv 0.34 0.710 1.000 2 2013 2014
dbSNP: rs8027411
rs8027411
4 0.882 0.040 15 79168687 intron variant G/T snv 0.52 0.710 1.000 1 2010 2010
dbSNP: rs10500355
rs10500355
3 0.925 0.040 16 7409346 intron variant T/A snv 0.29 0.700 1.000 1 2013 2013
dbSNP: rs10882165
rs10882165
2 1.000 10 93164567 intergenic variant A/T snv 0.39 0.700 1.000 1 2013 2013
dbSNP: rs11072826
rs11072826
1 15 79169174 intron variant A/G snv 0.40 0.700 1.000 1 2010 2010
dbSNP: rs11073058
rs11073058
3 1.000 0.040 15 34697425 regulatory region variant G/A;T snv 0.700 1.000 1 2010 2010
dbSNP: rs11073059
rs11073059
1 15 34697473 regulatory region variant T/A snv 0.41 0.700 1.000 1 2010 2010
dbSNP: rs11073060
rs11073060
2 1.000 0.040 15 34697650 intergenic variant C/A snv 0.41 0.700 1.000 1 2010 2010
dbSNP: rs11145465
rs11145465
2 1.000 9 69151677 missense variant C/A snv 0.19 0.700 1.000 1 2013 2013
dbSNP: rs11601239
rs11601239
2 1.000 11 105685872 intron variant C/G snv 0.48 0.700 1.000 1 2013 2013
dbSNP: rs11629665
rs11629665
1 15 79164791 intron variant G/A;C snv 0.52 0.700 1.000 1 2010 2010
dbSNP: rs11630571
rs11630571
1 15 79140650 downstream gene variant C/A snv 0.37 0.700 1.000 1 2010 2010
dbSNP: rs11631411
rs11631411
1 15 79153474 intron variant C/T snv 0.40 0.700 1.000 1 2010 2010
dbSNP: rs11634679
rs11634679
1 15 79140133 downstream gene variant T/C snv 0.38 0.700 1.000 1 2010 2010
dbSNP: rs11634903
rs11634903
1 15 79143850 intron variant A/C;G snv 0.700 1.000 1 2010 2010
dbSNP: rs11635757
rs11635757
1 15 79140395 downstream gene variant T/C snv 0.43 0.700 1.000 1 2010 2010
dbSNP: rs11638625
rs11638625
1 15 79142445 non coding transcript exon variant T/G snv 0.37 0.700 1.000 1 2010 2010
dbSNP: rs12205363
rs12205363
2 1.000 6 129513484 intron variant T/C;G snv 0.700 1.000 1 2013 2013
dbSNP: rs12229663
rs12229663
2 1.000 12 70856216 intron variant A/G;T snv 0.700 1.000 1 2013 2013
dbSNP: rs12439908
rs12439908
1 15 79164039 intron variant T/C snv 0.51 0.700 1.000 1 2010 2010
dbSNP: rs1254319
rs1254319
3 1.000 14 60437039 missense variant G/A snv 0.35 0.36 0.700 1.000 1 2013 2013
dbSNP: rs12902831
rs12902831
1 15 79140829 downstream gene variant G/A snv 0.42 0.700 1.000 1 2010 2010
dbSNP: rs12971120
rs12971120
2 1.000 18 74506788 intron variant A/G snv 0.20 0.700 1.000 1 2013 2013
dbSNP: rs14165
rs14165
2 1.000 3 53813381 3 prime UTR variant A/G;T snv 0.700 1.000 1 2013 2013