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: 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: 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: rs174544
rs174544
2 11 61800281 3 prime UTR variant C/A snv 0.25 0.700 1.000 1 2012 2012
dbSNP: rs174553
rs174553
2 1.000 0.040 11 61807686 intron variant A/G;T snv 0.28 0.700 1.000 1 2012 2012
dbSNP: rs174554
rs174554
7 1.000 0.080 11 61811991 intron variant A/G snv 0.40 0.28 0.700 1.000 1 2012 2012
dbSNP: rs174559
rs174559
3 11 61814184 non coding transcript exon variant G/A snv 0.23 0.700 1.000 1 2012 2012
dbSNP: rs174560
rs174560
5 1.000 0.080 11 61814292 non coding transcript exon variant T/C snv 0.30 0.700 1.000 1 2012 2012
dbSNP: rs174561
rs174561
3 1.000 0.080 11 61815236 5 prime UTR variant T/C snv 0.31 0.26 0.700 1.000 1 2012 2012
dbSNP: rs174562
rs174562
3 1.000 0.080 11 61817672 intron variant A/G snv 0.28 0.700 1.000 1 2012 2012
dbSNP: rs174566
rs174566
8 0.925 0.160 11 61824890 intron variant A/G snv 0.34 0.700 1.000 1 2012 2012
dbSNP: rs174568
rs174568
4 1.000 0.080 11 61826344 missense variant C/A;T snv 0.37 0.700 1.000 1 2012 2012
dbSNP: rs61897792
rs61897792
1 11 61819414 intron variant C/T snv 7.1E-02 0.700 1.000 1 2012 2012
dbSNP: rs968567
rs968567
7 0.851 0.240 11 61828092 intron variant C/T snv 0.11 0.700 1.000 1 2012 2012
dbSNP: rs99780
rs99780
3 1.000 0.080 11 61829161 intron variant C/T snv 0.38 0.700 1.000 1 2012 2012