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: rs7754840
rs7754840
3 0.807 0.200 6 20661019 intron variant G/A;C;T snv 0.900 0.958 8 2007 2019
dbSNP: rs7756992
rs7756992
4 0.827 0.240 6 20679478 intron variant A/G;T snv 0.900 0.966 5 2007 2019
dbSNP: rs10946398
rs10946398
3 0.827 0.160 6 20660803 intron variant A/C snv 0.40 0.900 1.000 3 2007 2019
dbSNP: rs4712523
rs4712523
3 0.925 0.120 6 20657333 intron variant A/G snv 0.41 0.830 1.000 3 2009 2019
dbSNP: rs9465871
rs9465871
3 0.882 0.120 6 20717024 intron variant T/C snv 0.30 0.830 1.000 3 2007 2017
dbSNP: rs10440833
rs10440833
1 1.000 0.080 6 20687890 intron variant T/A;G snv 0.26 0.820 1.000 4 2010 2019
dbSNP: rs6931514
rs6931514
3 0.925 0.120 6 20703721 intron variant A/G snv 0.27 0.820 1.000 2 2007 2012
dbSNP: rs4712524
rs4712524
2 0.925 0.120 6 20657634 intron variant A/G snv 0.40 0.820 1.000 1 2008 2019
dbSNP: rs9348440
rs9348440
2 1.000 0.080 6 20641105 intron variant C/T snv 0.13 0.800 1.000 3 2010 2013
dbSNP: rs7766070
rs7766070
3 1.000 0.080 6 20686342 intron variant C/A snv 0.25 0.800 1.000 2 2011 2016
dbSNP: rs9460550
rs9460550
1 1.000 0.080 6 20719330 intron variant G/A snv 0.30 0.800 1.000 1 2011 2019
dbSNP: rs9368222
rs9368222
5 1.000 0.080 6 20686765 intron variant C/A;T snv 0.700 1.000 4 2007 2012
dbSNP: rs1569699
rs1569699
1 1.000 0.080 6 20679079 intron variant T/G snv 0.41 0.700 1.000 3 2007 2011
dbSNP: rs10946403
rs10946403
1 1.000 0.080 6 20717173 intron variant A/G snv 0.30 0.700 1.000 2 2010 2011
dbSNP: rs2206734
rs2206734
3 0.882 0.160 6 20694653 intron variant C/T snv 0.20 0.700 1.000 2 2010 2011
dbSNP: rs2328531
rs2328531
1 1.000 0.080 6 20643521 intron variant A/G;T snv 0.700 1.000 2 2010 2011
dbSNP: rs2328548
rs2328548
1 1.000 0.080 6 20716727 intron variant G/A;T snv 0.700 1.000 2 2011 2012
dbSNP: rs6928012
rs6928012
1 1.000 0.080 6 20728282 intron variant C/T snv 0.49 0.700 1.000 2 2010 2011
dbSNP: rs7752906
rs7752906
1 1.000 0.080 6 20665824 intron variant G/A snv 0.40 0.700 1.000 2 2007 2011
dbSNP: rs9295475
rs9295475
1 1.000 0.080 6 20652534 intron variant A/G;T snv 0.700 1.000 2 2010 2011
dbSNP: rs9350271
rs9350271
1 1.000 0.080 6 20682933 intron variant G/A;C;T snv 0.700 1.000 2 2007 2011
dbSNP: rs9356744
rs9356744
3 0.882 0.120 6 20685255 intron variant T/C snv 0.42 0.700 1.000 2 2007 2011
dbSNP: rs9460540
rs9460540
1 1.000 0.080 6 20648531 intron variant A/G snv 0.35 0.700 1.000 2 2010 2011
dbSNP: rs9460546
rs9460546
1 1.000 0.080 6 20663401 intron variant T/G snv 0.40 0.700 1.000 2 2007 2011
dbSNP: rs979614
rs979614
1 1.000 0.080 6 20661892 intron variant A/G snv 0.35 0.700 1.000 2 2010 2011