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: rs2073398
rs2073398
1 22 24603137 intron variant C/G;T snv 0.800 1.000 1 2011 2011
dbSNP: rs4820599
rs4820599
6 0.925 0.160 22 24594246 intron variant A/G snv 0.43 0.700 1.000 2 2008 2011
dbSNP: rs2006092
rs2006092
1 22 24599701 intron variant A/G snv 0.51 0.700 1.000 1 2019 2019
dbSNP: rs2006227
rs2006227
2 22 24599789 intron variant C/A;T snv 0.700 1.000 1 2013 2013
dbSNP: rs2330795
rs2330795
1 22 24600615 intron variant G/A snv 0.42 0.700 1.000 1 2011 2011
dbSNP: rs5751901
rs5751901
1 22 24596299 intron variant T/C snv 0.39 0.700 1.000 1 2008 2008
dbSNP: rs5751902
rs5751902
2 1.000 0.080 22 24600663 intron variant C/T snv 0.29 0.700 1.000 1 2010 2010
dbSNP: rs6004193
rs6004193
1 22 24598329 intron variant T/A;C;G snv 0.700 1.000 1 2018 2018
dbSNP: rs9306395
rs9306395
1 22 24590177 intron variant G/A snv 0.29 0.700 1.000 1 2018 2018