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: rs1408579
rs1408579
3 1.000 0.040 10 100152437 intron variant C/T snv 0.32 0.700 1.000 1 2018 2018
dbSNP: rs12784396
rs12784396
4 0.925 0.040 10 100267650 5 prime UTR variant C/A;T snv 0.700 1.000 1 2018 2018
dbSNP: rs7222232
rs7222232
2 17 10033485 intron variant A/C snv 1.3E-02 0.700 1.000 1 2012 2012
dbSNP: rs8071787
rs8071787
5 17 10058819 intron variant T/C snv 4.8E-02 0.700 1.000 1 2012 2012
dbSNP: rs17158782
rs17158782
2 5 100726979 intergenic variant T/C snv 1.9E-02 0.700 1.000 1 2012 2012
dbSNP: rs17885778
rs17885778
2 7 100893830 missense variant G/A;C snv 4.0E-06; 1.0E-03 0.700 1.000 1 2012 2012
dbSNP: rs10185855
rs10185855
4 2 101025798 intron variant A/G snv 0.35 0.700 1.000 1 2018 2018
dbSNP: rs11571151
rs11571151
6 11 101127486 missense variant C/G;T snv 0.700 1.000 1 2012 2012
dbSNP: rs12097137
rs12097137
3 1 101243889 downstream gene variant G/A;T snv 0.700 1.000 1 2012 2012
dbSNP: rs2373459
rs2373459
1 12 101480178 intron variant C/T snv 0.68 0.700 1.000 1 2018 2018
dbSNP: rs1037116
rs1037116
2 15 101528701 upstream gene variant C/T snv 0.20 0.700 1.000 1 2018 2018
dbSNP: rs10107815
rs10107815
4 8 10156645 intron variant G/C snv 5.1E-02 0.700 1.000 1 2012 2012
dbSNP: rs6779158
rs6779158
2 3 10161878 upstream gene variant A/G snv 3.3E-02 0.700 1.000 1 2012 2012
dbSNP: rs17199964
rs17199964
5 4 101786634 intron variant G/A;C snv 0.700 1.000 1 2018 2018
dbSNP: rs13107325
rs13107325
34 0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02 0.800 1.000 4 2010 2018
dbSNP: rs13135092
rs13135092
4 4 102276925 intron variant A/G snv 5.1E-02 0.700 1.000 3 2015 2019
dbSNP: rs13114738
rs13114738
16 0.851 0.120 4 102363708 intron variant C/A;T snv 0.700 1.000 2 2016 2018
dbSNP: rs5742626
rs5742626
3 12 102464131 intron variant T/C snv 2.3E-02 0.700 1.000 1 2012 2012
dbSNP: rs7001567
rs7001567
4 8 10257027 intron variant C/G snv 3.7E-02 0.700 1.000 1 2012 2012
dbSNP: rs4648086
rs4648086
2 4 102600993 missense variant G/A snv 1.6E-03 2.9E-04 0.700 1.000 1 2012 2012
dbSNP: rs5030339
rs5030339
5 19 10269461 intron variant G/A snv 3.4E-03 0.700 1.000 1 2012 2012
dbSNP: rs5030361
rs5030361
4 19 10278833 intron variant C/T snv 6.8E-04 0.700 1.000 1 2012 2012
dbSNP: rs2075847
rs2075847
3 11 102799093 intron variant A/C;G snv 0.700 1.000 1 2012 2012
dbSNP: rs3025063
rs3025063
2 11 102840709 intron variant C/T snv 2.1E-02 0.700 1.000 1 2012 2012
dbSNP: rs11828157
rs11828157
5 11 102947395 intron variant G/A snv 4.7E-02 0.700 1.000 1 2012 2012