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: rs1045216
rs1045216
1 1.000 0.040 10 122429681 missense variant A/G snv 0.68 0.69 0.730 0.750 4 2013 2018
dbSNP: rs4146894
rs4146894
1 1.000 0.040 10 122395865 intron variant C/T snv 0.48 0.710 1.000 2 2007 2013
dbSNP: rs10510110
rs10510110
2 0.925 0.120 10 122432914 3 prime UTR variant T/C snv 0.56 0.700 1.000 2 2013 2013
dbSNP: rs2280141
rs2280141
4 1.000 0.040 10 122433665 3 prime UTR variant T/G snv 0.56 0.700 1.000 2 2013 2013
dbSNP: rs2292627
rs2292627
1 1.000 0.040 10 122442149 3 prime UTR variant T/G snv 0.11 0.700 1.000 2 2013 2013
dbSNP: rs2421016
rs2421016
3 0.925 0.120 10 122407996 intron variant C/T snv 0.46 0.700 1.000 2 2013 2013
dbSNP: rs7068487
rs7068487
2 0.925 0.120 10 122385696 intron variant C/T snv 0.31 0.700 1.000 2 2013 2013
dbSNP: rs7088058
rs7088058
5 0.851 0.040 10 122389836 intron variant C/T snv 0.32 0.700 1.000 2 2013 2013
dbSNP: rs10749466
rs10749466
1 1.000 0.040 10 122379288 intron variant A/G snv 0.32 0.700 1.000 1 2013 2013
dbSNP: rs10788284
rs10788284
1 1.000 0.040 10 122390401 intron variant T/C snv 0.55 0.700 1.000 1 2013 2013
dbSNP: rs10887149
rs10887149
1 1.000 0.040 10 122407488 intron variant G/A;C snv 0.700 1.000 1 2013 2013
dbSNP: rs10887150
rs10887150
1 1.000 0.040 10 122421062 non coding transcript exon variant C/A snv 0.47 0.700 1.000 1 2013 2013
dbSNP: rs10887151
rs10887151
1 1.000 0.040 10 122421250 non coding transcript exon variant C/T snv 0.45 0.700 1.000 1 2013 2013
dbSNP: rs11200594
rs11200594
1 1.000 0.040 10 122379877 intron variant C/T snv 0.47 0.700 1.000 1 2013 2013
dbSNP: rs11200595
rs11200595
1 1.000 0.040 10 122383113 intron variant T/A;C snv 0.700 1.000 1 2013 2013
dbSNP: rs11200604
rs11200604
1 1.000 0.040 10 122388123 intron variant G/A snv 0.47 0.700 1.000 1 2013 2013
dbSNP: rs11200629
rs11200629
1 1.000 0.040 10 122439069 3 prime UTR variant A/G snv 0.47 0.700 1.000 1 2013 2013
dbSNP: rs17103488
rs17103488
1 1.000 0.040 10 122394653 intron variant T/C snv 0.11 0.700 1.000 1 2013 2013
dbSNP: rs17103522
rs17103522
1 1.000 0.040 10 122418363 non coding transcript exon variant T/C snv 0.11 0.700 1.000 1 2013 2013
dbSNP: rs2292626
rs2292626
4 0.925 0.120 10 122427198 intron variant C/T snv 0.46 0.700 1.000 1 2013 2013
dbSNP: rs2421017
rs2421017
1 1.000 0.040 10 122388651 intron variant A/G snv 0.54 0.700 1.000 1 2013 2013
dbSNP: rs2421018
rs2421018
1 1.000 0.040 10 122388748 intron variant A/G snv 0.31 0.700 1.000 1 2013 2013
dbSNP: rs2421019
rs2421019
1 1.000 0.040 10 122391070 intron variant C/T snv 0.31 0.700 1.000 1 2013 2013
dbSNP: rs2421020
rs2421020
1 1.000 0.040 10 122391446 intron variant G/C snv 0.31 0.700 1.000 1 2013 2013
dbSNP: rs4311997
rs4311997
1 1.000 0.040 10 122419783 non coding transcript exon variant C/T snv 0.47 0.700 1.000 1 2013 2013