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: rs6570507
rs6570507
13 0.827 0.240 6 142358435 intron variant G/A snv 0.47 0.700 1.000 4 2009 2019
dbSNP: rs4896582
rs4896582
5 6 142382740 intron variant G/A snv 0.50 0.700 1.000 3 2008 2019
dbSNP: rs3748069
rs3748069
4 6 142446496 downstream gene variant A/G snv 0.39 0.700 1.000 2 2008 2019
dbSNP: rs7741741
rs7741741
6 0.925 0.040 6 142334664 intron variant T/A;G snv 0.700 1.000 2 2013 2019
dbSNP: rs6937121
rs6937121
3 6 142385996 intron variant T/G snv 0.47 0.700 1.000 1 2017 2017
dbSNP: rs7753012
rs7753012
5 6 142424746 intron variant T/G snv 0.50 0.700 1.000 1 2017 2017
dbSNP: rs9496369
rs9496369
1 6 142403781 intron variant C/T snv 0.33 0.41 0.700 1.000 1 2019 2019
dbSNP: rs972982
rs972982
3 6 142345724 intron variant T/C snv 0.44 0.700 1.000 1 2019 2019