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: rs174546
rs174546
17 0.807 0.200 11 61802358 3 prime UTR variant C/T snv 0.28 0.800 1.000 6 2009 2019
dbSNP: rs1535
rs1535
24 0.752 0.240 11 61830500 intron variant A/G snv 0.31 0.800 1.000 3 2012 2019
dbSNP: rs174548
rs174548
17 0.851 0.160 11 61803876 5 prime UTR variant C/G;T snv 0.800 1.000 2 2012 2019
dbSNP: rs174570
rs174570
11 0.882 0.200 11 61829740 intron variant C/T snv 0.15 0.800 1.000 2 2009 2019
dbSNP: rs174601
rs174601
12 0.925 0.080 11 61855668 non coding transcript exon variant C/A;T snv 0.800 1.000 2 2012 2018
dbSNP: rs174551
rs174551
6 11 61806212 5 prime UTR variant T/C snv 0.28 0.700 1.000 3 2015 2019
dbSNP: rs174554
rs174554
7 1.000 0.080 11 61811991 intron variant A/G snv 0.40 0.28 0.700 1.000 2 2018 2019
dbSNP: rs174583
rs174583
16 0.807 0.320 11 61842278 intron variant C/T snv 0.35 0.700 1.000 2 2018 2019
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 2019 2019
dbSNP: rs174549
rs174549
12 0.851 0.240 11 61803910 5 prime UTR variant G/A snv 0.26 0.700 1.000 1 2018 2018
dbSNP: rs174550
rs174550
13 0.925 0.160 11 61804006 5 prime UTR variant T/C snv 0.28 0.700 1.000 1 2018 2018
dbSNP: rs174566
rs174566
8 0.925 0.160 11 61824890 intron variant A/G snv 0.34 0.700 1.000 1 2019 2019
dbSNP: rs174568
rs174568
4 1.000 0.080 11 61826344 missense variant C/A;T snv 0.37 0.700 1.000 1 2019 2019
dbSNP: rs174574
rs174574
7 1.000 0.080 11 61832870 intron variant A/C snv 0.55 0.700 1.000 1 2016 2016
dbSNP: rs174576
rs174576
14 0.851 0.200 11 61836038 intron variant C/A;T snv 0.700 1.000 1 2012 2012
dbSNP: rs174577
rs174577
13 1.000 0.080 11 61837342 intron variant C/A snv 0.38 0.700 1.000 1 2018 2018