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: rs1040558
rs1040558
1 1.000 0.080 6 20713475 intron variant A/G snv 0.19 0.700 1.000 1 2011 2011
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: rs10946398
rs10946398
3 0.827 0.160 6 20660803 intron variant A/C snv 0.40 0.900 1.000 3 2007 2019
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: rs10946406
rs10946406
1 1.000 0.080 6 20758529 intron variant A/G;T snv 0.700 1.000 1 2011 2011
dbSNP: rs11753081
rs11753081
1 1.000 0.080 6 20705359 intron variant T/G snv 0.19 0.700 1.000 1 2011 2011
dbSNP: rs12111351
rs12111351
1 1.000 0.080 6 20724327 intron variant T/G snv 0.34 0.700 1.000 1 2011 2011
dbSNP: rs12664021
rs12664021
1 1.000 0.080 6 20760849 intron variant C/T snv 0.11 0.700 1.000 1 2011 2011
dbSNP: rs145494032
rs145494032
1 1.000 0.080 6 20665715 intron variant -/C delins 4.9E-05 0.700 1.000 1 2011 2011
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: rs2206734
rs2206734
3 0.882 0.160 6 20694653 intron variant C/T snv 0.20 0.700 1.000 2 2010 2011
dbSNP: rs2328529
rs2328529
1 1.000 0.080 6 20631722 intron variant C/A snv 0.19 0.700 1.000 1 2011 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: rs2328545
rs2328545
1 1.000 0.080 6 20653319 intron variant G/A;C snv 0.700 1.000 1 2011 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: rs2820001
rs2820001
1 1.000 0.080 6 20758712 intron variant G/T snv 0.85 0.700 1.000 1 2011 2011
dbSNP: rs4235999
rs4235999
1 1.000 0.080 6 20642991 intron variant C/G;T snv 0.39 0.700 1.000 1 2011 2011
dbSNP: rs4493738
rs4493738
1 1.000 0.080 6 20775429 intron variant A/G snv 7.5E-02 0.700 1.000 1 2011 2011
dbSNP: rs4710938
rs4710938
1 1.000 0.080 6 20640673 intron variant A/G snv 0.42 0.700 1.000 1 2011 2011
dbSNP: rs4710939
rs4710939
1 1.000 0.080 6 20644713 intron variant A/G snv 0.41 0.700 1.000 1 2011 2011
dbSNP: rs4710940
rs4710940
1 1.000 0.080 6 20657781 intron variant A/C snv 0.46 0.700 1.000 1 2011 2011
dbSNP: rs4712522
rs4712522
1 1.000 0.080 6 20656569 intron variant C/G snv 0.40 0.700 1.000 1 2011 2011
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: rs4712524
rs4712524
2 0.925 0.120 6 20657634 intron variant A/G snv 0.40 0.820 1.000 1 2008 2019
dbSNP: rs4712525
rs4712525
1 1.000 0.080 6 20662735 intron variant C/G;T snv 0.700 1.000 1 2011 2011