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: rs1064346
rs1064346
1 1.000 0.040 6 108043747 3 prime UTR variant T/C snv 0.25 0.700 1.000 1 2017 2017
dbSNP: rs12180499
rs12180499
1 1.000 0.040 6 108116042 intron variant A/G snv 0.700 1.000 1 2017 2017
dbSNP: rs12567
rs12567
1 1.000 0.040 6 108043378 3 prime UTR variant T/C snv 0.25 0.700 1.000 1 2017 2017
dbSNP: rs17069274
rs17069274
1 1.000 0.040 6 108124819 intron variant T/C snv 7.6E-02 0.700 1.000 1 2017 2017
dbSNP: rs2001144
rs2001144
1 1.000 0.040 6 108086458 intron variant A/C snv 0.25 0.700 1.000 1 2017 2017
dbSNP: rs2027876
rs2027876
1 1.000 0.040 6 108066028 intron variant G/A snv 0.27 0.700 1.000 1 2017 2017
dbSNP: rs218289
rs218289
1 1.000 0.040 6 108133233 intron variant A/G snv 0.29 0.700 1.000 1 2017 2017
dbSNP: rs218294
rs218294
1 1.000 0.040 6 108130689 intron variant A/G snv 0.41 0.700 1.000 1 2017 2017
dbSNP: rs4245535
rs4245535
1 1.000 0.040 6 108128008 intron variant C/T snv 6.4E-02 0.700 1.000 1 2017 2017
dbSNP: rs4946900
rs4946900
1 1.000 0.040 6 108094188 intron variant T/A;C snv 0.700 1.000 1 2017 2017
dbSNP: rs6919324
rs6919324
1 1.000 0.040 6 108121018 intron variant C/G;T snv 0.700 1.000 1 2017 2017
dbSNP: rs6921166
rs6921166
1 1.000 0.040 6 108072019 intron variant T/C snv 0.91 0.700 1.000 1 2017 2017
dbSNP: rs7769514
rs7769514
1 1.000 0.040 6 108091510 intron variant T/G snv 0.15 0.700 1.000 1 2017 2017
dbSNP: rs7769535
rs7769535
1 1.000 0.040 6 108091556 intron variant T/C snv 0.19 0.700 1.000 1 2017 2017
dbSNP: rs9320250
rs9320250
1 1.000 0.040 6 108044454 3 prime UTR variant T/C snv 0.41 0.700 1.000 1 2017 2017
dbSNP: rs9374013
rs9374013
1 1.000 0.040 6 108060143 intron variant G/A snv 0.23 0.700 1.000 1 2017 2017
dbSNP: rs9374021
rs9374021
1 1.000 0.040 6 108106220 intron variant G/A snv 0.72 0.700 1.000 1 2017 2017
dbSNP: rs9486815
rs9486815
1 1.000 0.040 6 108126842 intron variant G/A snv 0.42 0.700 1.000 1 2017 2017