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: rs12938031
rs12938031
6 0.851 0.160 17 45777136 intron variant A/G snv 0.26 0.700 1.000 1 2018 2018
dbSNP: rs1724422
rs1724422
2 1.000 0.040 17 45699947 intron variant A/G snv 0.47 0.700 1.000 1 2018 2018
dbSNP: rs34186148
rs34186148
2 1.000 0.040 17 45777289 intron variant G/A;C snv 0.31 0.700 1.000 1 2018 2018
dbSNP: rs35909029
rs35909029
2 1.000 0.040 17 45774132 intron variant T/A;C;G snv 0.700 1.000 1 2018 2018
dbSNP: rs62057061
rs62057061
2 1.000 0.040 17 45779273 intron variant C/G snv 0.14 0.700 1.000 1 2018 2018
dbSNP: rs7225384
rs7225384
2 1.000 0.040 17 45731730 non coding transcript exon variant C/G snv 0.39 0.700 1.000 1 2018 2018
dbSNP: rs9303521
rs9303521
5 0.925 0.120 17 45727828 intron variant T/C;G snv 0.60 0.700 1.000 1 2018 2018
dbSNP: rs110402
rs110402
12 0.790 0.120 17 45802681 intron variant G/A;C snv 0.030 1.000 3 2012 2016
dbSNP: rs242939
rs242939
3 0.882 0.120 17 45818213 intron variant C/T snv 0.86 0.030 1.000 3 2007 2013
dbSNP: rs242941
rs242941
9 0.790 0.200 17 45815154 intron variant A/C snv 0.62 0.030 1.000 3 2007 2013
dbSNP: rs12944712
rs12944712
3 0.925 0.040 17 45793781 intron variant G/A snv 0.35 0.010 1.000 1 2016 2016
dbSNP: rs173365
rs173365
3 0.882 0.080 17 45823708 intron variant A/G snv 0.55 0.010 1.000 1 2012 2012
dbSNP: rs1876828
rs1876828
4 0.851 0.160 17 45834159 intron variant C/T snv 0.14 0.010 1.000 1 2007 2007
dbSNP: rs242924
rs242924
3 0.882 0.080 17 45808001 intron variant G/T snv 0.44 0.010 1.000 1 2012 2012
dbSNP: rs4792888
rs4792888
2 0.925 0.040 17 45800588 non coding transcript exon variant A/G snv 0.17 0.010 1.000 1 2013 2013
dbSNP: rs7209436
rs7209436
5 0.851 0.200 17 45792776 intron variant C/T snv 0.43 0.010 1.000 1 2012 2012
dbSNP: rs878886
rs878886
3 0.925 0.080 17 45835124 3 prime UTR variant C/G;T snv 0.010 1.000 1 2016 2016