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: rs1535
rs1535
24 0.752 0.240 11 61830500 intron variant A/G snv 0.31 0.700 1.000 1 2011 2011
dbSNP: rs17156426
rs17156426
2 11 61841851 intron variant A/G;T snv 0.700 1.000 1 2011 2011
dbSNP: rs17156442
rs17156442
2 11 61846551 intron variant C/T snv 0.11 0.700 1.000 1 2011 2011
dbSNP: rs174541
rs174541
8 1.000 0.080 11 61798436 intron variant T/C snv 0.29 0.700 1.000 1 2011 2011
dbSNP: rs174547
rs174547
33 0.742 0.240 11 61803311 intron variant T/C snv 0.28 0.700 1.000 1 2011 2011
dbSNP: rs174548
rs174548
17 0.851 0.160 11 61803876 5 prime UTR variant C/G;T snv 0.700 1.000 1 2008 2008
dbSNP: rs174550
rs174550
13 0.925 0.160 11 61804006 5 prime UTR variant T/C snv 0.28 0.700 1.000 1 2011 2011
dbSNP: rs174556
rs174556
7 0.925 0.160 11 61813163 intron variant C/T snv 0.26 0.700 1.000 1 2011 2011
dbSNP: rs174570
rs174570
11 0.882 0.200 11 61829740 intron variant C/T snv 0.15 0.700 1.000 1 2011 2011
dbSNP: rs174574
rs174574
7 1.000 0.080 11 61832870 intron variant A/C snv 0.55 0.700 1.000 1 2011 2011
dbSNP: rs174575
rs174575
3 1.000 0.040 11 61834531 intron variant C/G snv 0.25 0.700 1.000 1 2011 2011
dbSNP: rs174579
rs174579
2 11 61838141 intron variant C/T snv 0.16 0.700 1.000 1 2011 2011
dbSNP: rs174583
rs174583
16 0.807 0.320 11 61842278 intron variant C/T snv 0.35 0.700 1.000 1 2011 2011
dbSNP: rs174585
rs174585
2 11 61844222 intron variant G/A;T snv 0.700 1.000 1 2011 2011
dbSNP: rs174589
rs174589
1 11 61848331 intron variant C/G;T snv 0.19 0.700 1.000 1 2011 2011
dbSNP: rs174591
rs174591
2 11 61850204 intron variant T/A;G snv 0.700 1.000 1 2011 2011
dbSNP: rs174593
rs174593
2 11 61851359 intron variant T/C snv 0.24 0.700 1.000 1 2011 2011
dbSNP: rs174597
rs174597
2 11 61853568 intron variant G/A;C;T snv 0.700 1.000 1 2011 2011
dbSNP: rs174602
rs174602
3 1.000 0.080 11 61856942 non coding transcript exon variant T/C snv 0.37 0.700 1.000 1 2011 2011
dbSNP: rs174605
rs174605
2 11 61859449 intron variant G/T snv 0.20 0.700 1.000 1 2011 2011
dbSNP: rs174611
rs174611
2 11 61860409 intron variant T/C snv 0.21 0.700 1.000 1 2011 2011
dbSNP: rs174616
rs174616
3 1.000 0.080 11 61861650 intron variant G/A snv 0.51 0.700 1.000 1 2011 2011
dbSNP: rs17764324
rs17764324
2 11 61867616 downstream gene variant G/A;T snv 0.700 1.000 1 2011 2011
dbSNP: rs17831757
rs17831757
2 11 61867728 downstream gene variant T/C snv 9.3E-02 0.700 1.000 1 2011 2011
dbSNP: rs2072114
rs2072114
4 1.000 0.080 11 61837743 intron variant A/G snv 0.19 0.16 0.700 1.000 1 2011 2011