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: rs13198118
rs13198118
4 1.000 6 30802955 intron variant T/G snv 0.17 0.700 1.000 2 2009 2010
dbSNP: rs4713380
rs4713380
5 0.925 0.120 6 30817496 intron variant T/C snv 0.17 0.700 1.000 2 2009 2010
dbSNP: rs4713385
rs4713385
5 0.925 0.120 6 30819816 intron variant G/A snv 0.17 0.700 1.000 2 2009 2010
dbSNP: rs2394403
rs2394403
4 1.000 6 30800092 intron variant C/T snv 0.17 0.700 1.000 1 2010 2010
dbSNP: rs4248149
rs4248149
4 1.000 6 30799850 intron variant T/C snv 0.17 0.700 1.000 1 2010 2010
dbSNP: rs4483030
rs4483030
4 1.000 6 30799352 intron variant C/T snv 0.20 0.700 1.000 1 2010 2010
dbSNP: rs4587207
rs4587207
5 1.000 6 30799168 intron variant A/G snv 0.17 0.700 1.000 1 2010 2010
dbSNP: rs4713383
rs4713383
4 1.000 6 30819464 intron variant G/A snv 0.17 0.700 1.000 1 2010 2010
dbSNP: rs4713389
rs4713389
4 1.000 6 30822827 intron variant G/T snv 0.17 0.700 1.000 1 2010 2010
dbSNP: rs4947290
rs4947290
4 1.000 6 30826628 intron variant G/A snv 0.17 0.700 1.000 1 2010 2010
dbSNP: rs6901761
rs6901761
4 1.000 6 30823021 intron variant C/T snv 0.17 0.700 1.000 1 2010 2010
dbSNP: rs6905957
rs6905957
4 1.000 6 30798963 intron variant A/G;T snv 0.700 1.000 1 2010 2010
dbSNP: rs7749924
rs7749924
4 1.000 6 30830214 intron variant C/T snv 0.12 0.700 1.000 1 2010 2010
dbSNP: rs7751869
rs7751869
4 1.000 6 30825537 intron variant A/G;T snv 0.700 1.000 1 2010 2010
dbSNP: rs9295924
rs9295924
5 0.925 0.120 6 30814584 non coding transcript exon variant G/A snv 0.27 0.17 0.700 1.000 1 2009 2009
dbSNP: rs9368644
rs9368644
4 1.000 6 30829306 intron variant C/T snv 0.17 0.700 1.000 1 2010 2010
dbSNP: rs9378109
rs9378109
5 0.925 0.120 6 30806697 intron variant C/A snv 0.16 0.700 1.000 1 2009 2009
dbSNP: rs9380198
rs9380198
4 1.000 6 30818109 intron variant G/T snv 0.17 0.700 1.000 1 2010 2010
dbSNP: rs9391696
rs9391696
4 1.000 6 30811009 intron variant A/G;T snv 0.700 1.000 1 2010 2010
dbSNP: rs9404974
rs9404974
4 1.000 6 30808706 intron variant T/C snv 0.17 0.700 1.000 1 2010 2010