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: rs9900280
rs9900280
1 17 29442580 intron variant G/A snv 0.58 0.800 1.000 1 2014 2014
dbSNP: rs191010498
rs191010498
1 17 29451055 intron variant C/T snv 7.0E-03 0.700 1.000 1 2016 2016
dbSNP: rs7208363
rs7208363
1 17 29406390 intron variant A/G;T snv 0.700 1.000 1 2012 2012
dbSNP: rs7209300
rs7209300
1 17 29518760 intron variant T/C;G snv 0.24 0.700 1.000 1 2016 2016
dbSNP: rs7213208
rs7213208
1 17 29405851 intron variant A/G;T snv 0.700 1.000 1 2012 2012
dbSNP: rs9891920
rs9891920
1 17 29446271 intron variant A/G;T snv 0.700 1.000 1 2016 2016