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: rs1505307
rs1505307
6 3 24301839 intron variant T/C snp 0.61 0.800 2 2012 2017
dbSNP: rs9310736
rs9310736
4 3 24309320 intron variant A/G snp 0.70 0.800 2 2010 2012
dbSNP: rs113700287
rs113700287
5 3 24293020 intron variant T/TTTG,TTTTC,TTTTG in-del 3.2E-05; 0.72 0.700 1 2017 2017
dbSNP: rs1158265
rs1158265
2 3 24294671 intron variant T/C snp 0.33 0.700 1 2012 2012
dbSNP: rs12485694
rs12485694
2 3 24304618 intron variant A/G,T snp 0.57 0.700 1 2012 2012
dbSNP: rs1505283
rs1505283
2 3 24304285 intron variant A/G snp 0.57 0.700 1 2012 2012
dbSNP: rs1505297
rs1505297
2 3 24314143 intron variant T/A,C snp 0.57 0.700 1 2012 2012
dbSNP: rs1868575
rs1868575
2 3 24288792 intron variant G/A snp 0.49 0.700 1 2012 2012
dbSNP: rs2167115
rs2167115
2 3 24298243 intron variant A/G snp 0.47 0.700 1 2012 2012
dbSNP: rs7610039
rs7610039
2 3 24315591 intron variant T/C snp 0.59 0.700 1 2012 2012
dbSNP: rs7610222
rs7610222
2 3 24315795 intron variant T/C snp 0.74 0.700 1 2012 2012
dbSNP: rs7622481
rs7622481
2 3 24310380 intron variant C/T snp 0.27 0.700 1 2012 2012
dbSNP: rs7640580
rs7640580
2 3 24315752 intron variant C/A snp 0.70 0.700 1 2012 2012
dbSNP: rs9830674
rs9830674
2 3 24296423 intron variant C/T snp 0.33 0.700 1 2012 2012