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: rs6859
rs6859
10 0.827 0.120 19 44878777 3 prime UTR variant A/G snv 0.58 0.800 1.000 2 2012 2019
dbSNP: rs283813
rs283813
6 1.000 0.080 19 44885917 intron variant T/A snv 0.11 0.16 0.700 1.000 2 2012 2012
dbSNP: rs7254892
rs7254892
4 19 44886339 intron variant G/A snv 6.4E-02 0.700 1.000 2 2019 2019
dbSNP: rs2075642
rs2075642
3 19 44874210 intron variant G/A;T snv 0.700 1.000 1 2012 2012
dbSNP: rs3852856
rs3852856
3 19 44858317 intron variant G/A;C;T snv 0.700 1.000 1 2012 2012
dbSNP: rs387976
rs387976
4 1.000 0.080 19 44875803 intron variant A/C;T snv 0.700 1.000 1 2012 2012
dbSNP: rs395908
rs395908
2 19 44870308 intron variant G/A snv 0.16 0.700 1.000 1 2018 2018
dbSNP: rs41290120
rs41290120
3 1.000 0.080 19 44879418 intron variant G/A;T snv 0.700 1.000 1 2019 2019
dbSNP: rs4803763
rs4803763
4 1.000 0.080 19 44854034 intron variant G/A;C snv 0.700 1.000 1 2012 2012
dbSNP: rs4803766
rs4803766
2 19 44867911 intron variant G/A snv 0.44 0.700 1.000 1 2012 2012
dbSNP: rs519113
rs519113
6 1.000 0.080 19 44873027 intron variant C/G;T snv 0.700 1.000 1 2012 2012
dbSNP: rs6857
rs6857
16 0.790 0.240 19 44888997 3 prime UTR variant C/T snv 0.13 0.700 1.000 1 2012 2012
dbSNP: rs8104483
rs8104483
3 19 44869097 intron variant T/G snv 0.28 0.700 1.000 1 2012 2012