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: rs1158265
rs1158265
1 3 24294671 intron variant T/C snv 0.32 0.700 1.000 1 2012 2012
dbSNP: rs12485694
rs12485694
1 3 24304618 intron variant A/G;T snv 0.700 1.000 1 2012 2012
dbSNP: rs1505283
rs1505283
1 3 24304285 intron variant A/G snv 0.56 0.700 1.000 1 2012 2012
dbSNP: rs1505297
rs1505297
1 3 24314143 intron variant T/A;C snv 0.700 1.000 1 2012 2012
dbSNP: rs1505307
rs1505307
7 3 24301839 intron variant T/C snv 0.60 0.700 1.000 1 2012 2012
dbSNP: rs1868575
rs1868575
1 3 24288792 intron variant G/A snv 0.48 0.700 1.000 1 2012 2012
dbSNP: rs2167115
rs2167115
1 3 24298243 intron variant A/G snv 0.47 0.700 1.000 1 2012 2012
dbSNP: rs7610039
rs7610039
1 3 24315591 intron variant T/C snv 0.59 0.700 1.000 1 2012 2012
dbSNP: rs7610222
rs7610222
1 3 24315795 intron variant T/C snv 0.73 0.700 1.000 1 2012 2012
dbSNP: rs7622481
rs7622481
1 3 24310380 intron variant C/T snv 0.27 0.700 1.000 1 2012 2012
dbSNP: rs7640580
rs7640580
1 3 24315752 intron variant C/A snv 0.70 0.700 1.000 1 2012 2012
dbSNP: rs869784
rs869784
3 3 24306517 intron variant T/C snv 0.68 0.700 1.000 1 2016 2016
dbSNP: rs9310736
rs9310736
4 3 24309320 intron variant A/G snv 0.69 0.700 1.000 1 2012 2012
dbSNP: rs9830674
rs9830674
1 3 24296423 intron variant C/T snv 0.33 0.700 1.000 1 2012 2012