Source: ALL
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: rs1889891
rs1889891
1 1.000 0.040 6 129492201 non coding transcript exon variant C/T snv 0.37 0.010 1.000 1 2016 2016
dbSNP: rs200329677
rs200329677
1 1.000 0.040 22 45973898 intron variant C/T snv 1.4E-05 0.010 1.000 1 2018 2018
dbSNP: rs201140091
rs201140091
1 1.000 0.040 10 48200198 intron variant A/-;AAAAA;AAAAAA;AAAAAAAAA;AAAAAAAAAA;AAAAAAAAAAA;AAAAAAAAAAAAA;AAAAAAAAAAAAAA delins 0.700 1.000 1 2016 2016
dbSNP: rs2071754
rs2071754
1 1.000 0.040 11 31791034 non coding transcript exon variant C/G;T snv 0.010 1.000 1 2018 2018
dbSNP: rs2155413
rs2155413
1 1.000 0.040 11 84923746 intron variant C/A snv 0.55 0.700 1.000 1 2016 2016
dbSNP: rs2181346
rs2181346
1 1.000 0.040 14 54085710 regulatory region variant A/T snv 0.23 0.700 1.000 1 2016 2016
dbSNP: rs2207136
rs2207136
1 1.000 0.040 6 50842007 intron variant T/C snv 0.34 0.700 1.000 1 2016 2016
dbSNP: rs2218817
rs2218817
1 1.000 0.040 4 111689850 regulatory region variant G/A snv 0.32 0.010 1.000 1 2012 2012
dbSNP: rs2342406
rs2342406
1 1.000 0.040 2 44925609 intron variant T/C snv 0.19 0.700 1.000 1 2016 2016
dbSNP: rs2799081
rs2799081
1 1.000 0.040 6 28302807 downstream gene variant T/C snv 0.41 0.700 1.000 1 2016 2016
dbSNP: rs2808510
rs2808510
1 1.000 0.040 1 200366947 non coding transcript exon variant C/T snv 0.29 0.700 1.000 1 2016 2016
dbSNP: rs2839471
rs2839471
1 1.000 0.040 21 42134346 intron variant C/T snv 0.39 0.010 < 0.001 1 2011 2011
dbSNP: rs2853559
rs2853559
VDR
1 1.000 0.040 12 47889022 intron variant A/G snv 0.68 0.010 1.000 1 2011 2011
dbSNP: rs2908972
rs2908972
1 1.000 0.040 17 11503942 intron variant T/A snv 0.39 0.700 1.000 1 2016 2016
dbSNP: rs297589
rs297589
1 1.000 0.040 2 156502238 intron variant T/A snv 0.65 0.700 1.000 1 2016 2016
dbSNP: rs34016308
rs34016308
1 1.000 0.040 14 92149397 intron variant -/TA delins 0.19 0.700 1.000 1 2016 2016
dbSNP: rs34217772
rs34217772
1 1.000 0.040 14 41804367 intron variant C/G snv 0.16 0.700 1.000 1 2016 2016
dbSNP: rs3760753
rs3760753
1 1.000 0.040 19 10011783 upstream gene variant G/A;T snv 0.010 1.000 1 2010 2010
dbSNP: rs479445
rs479445
1 1.000 0.040 1 60875960 intron variant T/A snv 0.31 0.700 1.000 1 2016 2016
dbSNP: rs4948523
rs4948523
1 1.000 0.040 10 58579338 intron variant A/C snv 0.51 0.700 1.000 1 2016 2016
dbSNP: rs5022942
rs5022942
1 1.000 0.040 4 81038812 intron variant A/G snv 0.59 0.700 1.000 1 2016 2016
dbSNP: rs56299331
rs56299331
1 1.000 0.040 10 113028677 intron variant C/T snv 0.15 0.700 1.000 1 2016 2016
dbSNP: rs5742629
rs5742629
1 1.000 0.040 12 102463485 non coding transcript exon variant T/C snv 0.32 0.010 1.000 1 2012 2012
dbSNP: rs61049169
rs61049169
1 1.000 0.040 2 146131140 intergenic variant G/A;C snv 0.700 1.000 1 2016 2016
dbSNP: rs6837348
rs6837348
1 1.000 0.040 4 111787647 intergenic variant G/A snv 0.28 0.010 1.000 1 2012 2012