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: rs121434592
rs121434592
54 0.595 0.640 14 104780214 missense variant C/T snv 4.0E-06 0.770 1.000 7 2008 2019
dbSNP: rs2494740
rs2494740
2 0.925 0.080 14 104781544 intron variant A/T snv 0.61 0.010 1.000 1 2018 2018
dbSNP: rs2494744
rs2494744
2 0.925 0.080 14 104789477 intron variant A/G snv 0.83 0.010 1.000 1 2018 2018
dbSNP: rs2494752
rs2494752
10 0.790 0.120 14 104797271 upstream gene variant A/G snv 0.85 0.010 1.000 1 2017 2017
dbSNP: rs2498789
rs2498789
2 0.925 0.080 14 104783708 intron variant A/G snv 0.26 0.010 1.000 1 2018 2018
dbSNP: rs3730358
rs3730358
14 0.724 0.360 14 104780070 intron variant G/A;C snv 0.16; 4.0E-03 0.010 1.000 1 2018 2018
dbSNP: rs3803304
rs3803304
3 0.882 0.160 14 104772809 intron variant C/G snv 0.24 0.010 1.000 1 2018 2018