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: rs9818870
rs9818870
9 0.807 0.200 3 138403280 3 prime UTR variant C/A;T snv 0.740 0.600 5 2011 2019
dbSNP: rs139016349
rs139016349
1 1.000 0.040 3 138380319 intron variant -/CTT delins 0.21 0.700 1.000 1 2017 2017
dbSNP: rs185244
rs185244
1 1.000 0.040 3 138374047 intron variant C/T snv 0.19 0.700 1.000 1 2018 2018
dbSNP: rs2306374
rs2306374
2 0.925 0.040 3 138401110 intron variant T/C snv 0.12 0.700 1.000 1 2013 2013
dbSNP: rs3732837
rs3732837
1 1.000 0.040 3 138403078 3 prime UTR variant A/G;T snv 0.700 1.000 1 2018 2018
dbSNP: rs1199337
rs1199337
1 1.000 0.040 3 138369222 intron variant G/C snv 0.19 0.010 1.000 1 2015 2015
dbSNP: rs1720819
rs1720819
1 1.000 0.040 3 138381697 intron variant T/G snv 0.18 0.010 1.000 1 2013 2013
dbSNP: rs253662
rs253662
1 1.000 0.040 3 138378471 intron variant T/C snv 0.84 0.010 1.000 1 2013 2013
dbSNP: rs6782181
rs6782181
6 0.851 0.160 3 138386212 intron variant G/A;C snv 0.010 1.000 1 2013 2013