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: rs6459467
rs6459467
3 6 16287961 intron variant G/A;C snv 0.800 1.000 2 2012 2016
dbSNP: rs1042391
rs1042391
1 6 16290530 missense variant T/A;C snv 0.54 0.700 1.000 1 2012 2012
dbSNP: rs11969354
rs11969354
1 6 16289097 intron variant G/A;C snv 0.700 1.000 1 2012 2012
dbSNP: rs13215954
rs13215954
1 6 16294807 intron variant C/A snv 0.20 0.700 1.000 1 2012 2012
dbSNP: rs3814453
rs3814453
1 6 16236606 upstream gene variant T/G snv 0.15 0.700 1.000 1 2012 2012
dbSNP: rs4716056
rs4716056
1 6 16278159 intron variant A/G snv 0.49 0.700 1.000 1 2012 2012
dbSNP: rs4716058
rs4716058
1 6 16291944 intron variant C/T snv 0.14 0.700 1.000 1 2012 2012
dbSNP: rs4716059
rs4716059
1 6 16292529 intron variant C/T snv 0.14 0.700 1.000 1 2012 2012
dbSNP: rs6459465
rs6459465
1 6 16247899 intron variant G/C snv 0.56 0.700 1.000 1 2012 2012
dbSNP: rs6723
rs6723
1 6 16295358 3 prime UTR variant C/G snv 0.49 0.700 1.000 1 2012 2012
dbSNP: rs6914805
rs6914805
2 6 16280956 intron variant C/T snv 0.33 0.700 1.000 1 2012 2012
dbSNP: rs6922229
rs6922229
1 6 16275469 intron variant C/G;T snv 0.700 1.000 1 2012 2012
dbSNP: rs6926552
rs6926552
1 6 16290631 intron variant T/A;C snv 0.24 0.700 1.000 1 2012 2012
dbSNP: rs6933491
rs6933491
1 6 16268177 intron variant A/G;T snv 0.700 1.000 1 2012 2012
dbSNP: rs7742883
rs7742883
1 6 16257985 non coding transcript exon variant A/G snv 0.56 0.700 1.000 1 2012 2012
dbSNP: rs7752579
rs7752579
1 6 16251828 intron variant T/A;C snv 0.700 1.000 1 2018 2018
dbSNP: rs7763322
rs7763322
1 6 16253864 intron variant T/C snv 0.56 0.700 1.000 1 2012 2012
dbSNP: rs7765828
rs7765828
3 6 16294491 intron variant C/G snv 0.56 0.700 1.000 1 2012 2012
dbSNP: rs9350003
rs9350003
1 6 16289080 intron variant T/A snv 0.14 0.700 1.000 1 2012 2012
dbSNP: rs9383138
rs9383138
1 6 16239548 intron variant G/A snv 0.26 0.700 1.000 1 2012 2012
dbSNP: rs9396658
rs9396658
1 6 16252622 intron variant T/C snv 0.33 0.700 1.000 1 2012 2012
dbSNP: rs9396661
rs9396661
1 6 16274560 intron variant G/A snv 0.27 0.700 1.000 1 2012 2012
dbSNP: rs9477074
rs9477074
3 6 16269132 intron variant T/C snv 0.54 0.700 1.000 1 2012 2012