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: rs2531995
rs2531995
7 1.000 0.080 16 3963466 3 prime UTR variant C/T snv 0.45 0.700 1.000 5 2014 2019
dbSNP: rs879620
rs879620
3 16 3965728 3 prime UTR variant C/T snv 0.49 0.46 0.700 1.000 2 2017 2018
dbSNP: rs2238435
rs2238435
1 16 3964281 3 prime UTR variant C/A;G;T snv 0.700 1.000 1 2019 2019
dbSNP: rs2444217
rs2444217
3 16 3988386 intron variant G/A snv 0.45 0.700 1.000 1 2010 2010
dbSNP: rs2540034
rs2540034
1 16 3972693 intron variant C/T snv 0.43 0.700 1.000 1 2017 2017
dbSNP: rs2601777
rs2601777
1 16 3985067 intron variant A/G snv 0.59 0.700 1.000 1 2019 2019
dbSNP: rs7185966
rs7185966
3 16 3972702 intron variant G/A snv 0.26 0.700 1.000 1 2019 2019