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: rs4712524
rs4712524
2 0.925 0.120 6 20657634 intron variant A/G snv 0.40 0.820 1.000 1 2008 2019
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: rs6906327
rs6906327
1 1.000 0.080 6 20659228 intron variant G/A snv 0.47 0.700 1.000 1 2011 2011
dbSNP: rs6456367
rs6456367
1 1.000 0.080 6 20659356 intron variant T/A snv 0.40 0.700 1.000 1 2011 2011
dbSNP: rs6456368
rs6456368
2 1.000 0.080 6 20659575 intron variant T/C snv 0.40 0.700 1.000 1 2011 2011
dbSNP: rs6456369
rs6456369
1 1.000 0.080 6 20660134 intron variant T/A;C;G snv 0.700 1.000 1 2011 2011
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: rs7774594
rs7774594
1 1.000 0.080 6 20660912 intron variant T/A snv 0.40 0.700 1.000 1 2011 2011
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: rs9460544
rs9460544
1 1.000 0.080 6 20661298 intron variant G/A;T snv 0.700 1.000 1 2011 2011
dbSNP: rs9460545
rs9460545
1 1.000 0.080 6 20661319 intron variant T/A;C snv 0.700 1.000 1 2011 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
dbSNP: rs4712525
rs4712525
1 1.000 0.080 6 20662735 intron variant C/G;T snv 0.700 1.000 1 2011 2011
dbSNP: rs4712526
rs4712526
1 1.000 0.080 6 20662804 intron variant T/A snv 0.40 0.700 1.000 1 2011 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: rs742642
rs742642
1 1.000 0.080 6 20664850 intron variant G/A snv 0.21 0.700 1.000 1 2011 2011
dbSNP: rs7748382
rs7748382
1 1.000 0.080 6 20665318 intron variant G/A snv 0.41 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: rs7772603
rs7772603
1 1.000 0.080 6 20665715 intron variant T/C snv 0.40 0.700 1.000 1 2011 2011
dbSNP: rs7752780
rs7752780
1 1.000 0.080 6 20665791 intron variant G/A snv 0.40 0.700 1.000 1 2011 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: rs9358356
rs9358356
1 1.000 0.080 6 20667151 intron variant T/C snv 0.39 0.700 1.000 1 2011 2011
dbSNP: rs9350270
rs9350270
1 1.000 0.080 6 20667568 intron variant A/G;T snv 0.700 1.000 1 2011 2011
dbSNP: rs9368219
rs9368219
3 1.000 0.080 6 20674460 intron variant C/T snv 0.19 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