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
10 0.752 0.240 11 61830500 intron variant A/G snv 0.31 0.800 1.000 2 2010 2019
dbSNP: rs174546
rs174546
9 0.807 0.200 11 61802358 3 prime UTR variant C/T snv 0.28 0.800 1.000 2 2010 2019
dbSNP: rs174548
rs174548
9 0.851 0.160 11 61803876 5 prime UTR variant C/G;T snv 0.800 1.000 2 2010 2012
dbSNP: rs174547
rs174547
10 0.742 0.240 11 61803311 intron variant T/C snv 0.28 0.800 1.000 1 2009 2019
dbSNP: rs174577
rs174577
5 1.000 0.080 11 61837342 intron variant C/A snv 0.38 0.800 1.000 1 2012 2018
dbSNP: rs174601
rs174601
8 0.925 0.080 11 61855668 non coding transcript exon variant C/A;T snv 0.800 1.000 1 2012 2018
dbSNP: rs174570
rs174570
10 0.882 0.200 11 61829740 intron variant C/T snv 0.15 0.700 1.000 1 2012 2012
dbSNP: rs174576
rs174576
9 0.851 0.200 11 61836038 intron variant C/A;T snv 0.700 1.000 1 2012 2012