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: rs1049353
rs1049353
42 0.630 0.600 6 88143916 synonymous variant C/T snv 0.21 0.20 0.030 0.667 3 2002 2013
dbSNP: rs12720071
rs12720071
7 0.807 0.200 6 88141462 3 prime UTR variant T/C snv 0.11 0.020 1.000 2 2011 2013
dbSNP: rs2023239
rs2023239
20 0.724 0.160 6 88150763 intron variant T/C snv 0.21 0.010 1.000 1 2015 2015
dbSNP: rs4707436
rs4707436
1 1.000 0.040 6 88142032 3 prime UTR variant G/A snv 0.31 0.010 1.000 1 2013 2013
dbSNP: rs806368
rs806368
14 0.752 0.280 6 88140381 3 prime UTR variant T/C snv 0.19 0.010 1.000 1 2013 2013
dbSNP: rs9444584
rs9444584
4 0.882 0.160 6 88152840 intron variant C/T snv 0.30 0.010 1.000 1 2012 2012