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 0.050 1.000 5 2007 2018
dbSNP: rs2023239
rs2023239
20 0.724 0.160 6 88150763 intron variant T/C snv 0.21 0.020 1.000 2 2012 2012
dbSNP: rs806368
rs806368
14 0.752 0.280 6 88140381 3 prime UTR variant T/C snv 0.19 0.010 1.000 1 2010 2010
dbSNP: rs806381
rs806381
2 0.925 0.080 6 88156182 intron variant A/G snv 0.32 0.010 1.000 1 2012 2012
dbSNP: rs9444584
rs9444584
4 0.882 0.160 6 88152840 intron variant C/T snv 0.30 0.010 1.000 1 2012 2012
dbSNP: rs9450898
rs9450898
3 0.925 0.160 6 88154344 intron variant C/T snv 0.21 0.010 1.000 1 2012 2012