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 0.700 1.000 3 2009 2013
dbSNP: rs1535
rs1535
24 0.752 0.240 11 61830500 intron variant A/G snv 0.31 0.700 1.000 1 2012 2012
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: rs174548
rs174548
17 0.851 0.160 11 61803876 5 prime UTR variant C/G;T snv 0.700 1.000 1 2012 2012
dbSNP: rs174570
rs174570
11 0.882 0.200 11 61829740 intron variant C/T snv 0.15 0.700 1.000 1 2009 2009
dbSNP: rs174576
rs174576
14 0.851 0.200 11 61836038 intron variant C/A;T snv 0.700 1.000 1 2012 2012
dbSNP: rs174601
rs174601
12 0.925 0.080 11 61855668 non coding transcript exon variant C/A;T snv 0.700 1.000 1 2012 2012