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: rs724016
rs724016
5 1.000 0.040 3 141386728 5 prime UTR variant A/G snv 0.52 0.700 1.000 6 2008 2019
dbSNP: rs6763931
rs6763931
4 0.925 0.080 3 141383991 intron variant G/A snv 0.54 0.700 1.000 4 2008 2019
dbSNP: rs1991431
rs1991431
4 3 141414608 intron variant G/A snv 0.50 0.700 1.000 3 2013 2019
dbSNP: rs6440003
rs6440003
4 3 141375367 intron variant G/A snv 0.54 0.700 1.000 3 2008 2019
dbSNP: rs10513137
rs10513137
2 3 141424588 intron variant G/A;C snv 0.700 1.000 2 2009 2010
dbSNP: rs114097136
rs114097136
1 3 141395171 intron variant C/G snv 3.6E-02 0.700 1.000 1 2017 2017
dbSNP: rs1346408
rs1346408
2 3 141353447 intron variant C/T snv 0.55 0.700 1.000 1 2019 2019
dbSNP: rs200235318
rs200235318
1 3 141394029 intron variant TG/- del 0.700 1.000 1 2017 2017
dbSNP: rs28721484
rs28721484
2 3 141334437 intron variant C/T snv 0.22 0.700 1.000 1 2017 2017
dbSNP: rs55768579
rs55768579
1 3 141340945 intron variant GA/- delins 1.3E-03 0.700 1.000 1 2017 2017
dbSNP: rs74888405
rs74888405
1 3 141399390 intron variant T/C snv 4.9E-02 0.700 1.000 1 2019 2019
dbSNP: rs9825379
rs9825379
2 3 141418193 intron variant G/A snv 0.13 0.700 1.000 1 2010 2010