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: rs2240335
rs2240335
1 1.000 0.120 1 17348042 synonymous variant C/A snv 0.39 0.37 0.810 1.000 3 2011 2019
dbSNP: rs2301888
rs2301888
1 1.000 0.120 1 17346235 intron variant G/A snv 0.31 0.800 1.000 3 2014 2019
dbSNP: rs2240336
rs2240336
1 1.000 0.120 1 17347907 intron variant C/T snv 0.43 0.45 0.800 1.000 1 2012 2012
dbSNP: rs2240339
rs2240339
1 1.000 0.120 1 17347613 intron variant C/T snv 0.36 0.800 1.000 1 2012 2012
dbSNP: rs2240340
rs2240340
1 1.000 0.120 1 17336144 intron variant T/C snv 0.56 0.54 0.770 1.000 7 2008 2017
dbSNP: rs11203366
rs11203366
2 0.925 0.200 1 17331039 missense variant G/A snv 0.56 0.55 0.720 1.000 3 2007 2017
dbSNP: rs11203368
rs11203368
3 0.925 0.200 1 17340013 intron variant C/T snv 0.57 0.700 1.000 1 2011 2011
dbSNP: rs1748033
rs1748033
2 0.925 0.120 1 17336167 missense variant T/C;G snv 0.63; 4.0E-06 0.030 1.000 3 2014 2018
dbSNP: rs11203367
rs11203367
1 1.000 0.120 1 17331121 missense variant T/C snv 0.56 0.56 0.020 1.000 2 2007 2017
dbSNP: rs874881
rs874881
1 1.000 0.120 1 17334004 missense variant G/C;T snv 0.55; 1.2E-05 0.020 1.000 2 2007 2017