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: rs1260326
rs1260326
81 0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 0.800 1.000 5 2010 2018
dbSNP: rs174548
rs174548
17 0.851 0.160 11 61803876 5 prime UTR variant C/G;T snv 0.700 1.000 3 2008 2013
dbSNP: rs4775041
rs4775041
8 1.000 0.040 15 58382496 intron variant G/C snv 0.24 0.700 1.000 3 2008 2013
dbSNP: rs102275
rs102275
18 0.827 0.320 11 61790331 non coding transcript exon variant T/C snv 0.47 0.700 1.000 2 2012 2013
dbSNP: rs10468017
rs10468017
12 0.851 0.120 15 58386313 intron variant C/T snv 0.24 0.700 1.000 2 2012 2013
dbSNP: rs108499
rs108499
2 11 61779765 intron variant C/T snv 0.27 0.700 1.000 2 2012 2013
dbSNP: rs1535
rs1535
24 0.752 0.240 11 61830500 intron variant A/G snv 0.31 0.700 1.000 2 2012 2013
dbSNP: rs174449
rs174449
2 11 61872907 downstream gene variant G/A snv 0.54 0.700 1.000 2 2012 2013
dbSNP: rs174455
rs174455
5 1.000 0.080 11 61888645 intron variant G/A;C snv 0.700 1.000 2 2012 2013
dbSNP: rs174528
rs174528
5 1.000 0.080 11 61776027 intron variant T/C snv 0.42 0.42 0.700 1.000 2 2012 2013
dbSNP: rs174534
rs174534
3 1.000 0.080 11 61781986 non coding transcript exon variant A/G snv 0.28 0.700 1.000 2 2012 2013
dbSNP: rs174535
rs174535
19 0.776 0.280 11 61783884 missense variant T/A;C;G snv 0.38 0.32 0.700 1.000 2 2012 2013
dbSNP: rs174536
rs174536
3 11 61784455 non coding transcript exon variant A/C snv 0.29 0.700 1.000 2 2012 2013
dbSNP: rs174537
rs174537
23 0.708 0.400 11 61785208 non coding transcript exon variant G/T snv 0.28 0.700 1.000 2 2012 2013
dbSNP: rs174538
rs174538
21 0.701 0.440 11 61792609 5 prime UTR variant G/A snv 0.34 0.26 0.700 1.000 2 2012 2013
dbSNP: rs174541
rs174541
8 1.000 0.080 11 61798436 intron variant T/C snv 0.29 0.700 1.000 2 2012 2013
dbSNP: rs174545
rs174545
5 1.000 0.080 11 61801834 3 prime UTR variant C/A;G snv 0.28 0.700 1.000 2 2012 2013
dbSNP: rs174546
rs174546
17 0.807 0.200 11 61802358 3 prime UTR variant C/T snv 0.28 0.700 1.000 2 2012 2013
dbSNP: rs174547
rs174547
33 0.742 0.240 11 61803311 intron variant T/C snv 0.28 0.700 1.000 2 2010 2013
dbSNP: rs174549
rs174549
12 0.851 0.240 11 61803910 5 prime UTR variant G/A snv 0.26 0.700 1.000 2 2012 2013
dbSNP: rs174550
rs174550
13 0.925 0.160 11 61804006 5 prime UTR variant T/C snv 0.28 0.700 1.000 2 2012 2013
dbSNP: rs174555
rs174555
4 11 61812288 intron variant T/C snv 0.26 0.700 1.000 2 2012 2013
dbSNP: rs174556
rs174556
7 0.925 0.160 11 61813163 intron variant C/T snv 0.26 0.700 1.000 2 2012 2013
dbSNP: rs174570
rs174570
11 0.882 0.200 11 61829740 intron variant C/T snv 0.15 0.700 1.000 2 2012 2013
dbSNP: rs174576
rs174576
14 0.851 0.200 11 61836038 intron variant C/A;T snv 0.700 1.000 2 2012 2013