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: rs61755320
rs61755320
41 0.716 0.520 16 89546737 missense variant C/T snv 2.9E-03 3.5E-03 0.700 0
dbSNP: rs10046257
rs10046257
1 1.000 0.040 6 32886920 regulatory region variant G/A snv 0.15 0.800 1.000 1 2013 2013
dbSNP: rs10214886
rs10214886
1 1.000 0.040 6 32889642 intergenic variant T/A snv 0.14 0.800 1.000 1 2013 2013
dbSNP: rs1029295
rs1029295
1 1.000 0.040 6 32888705 intergenic variant T/C snv 0.14 0.800 1.000 1 2013 2013
dbSNP: rs1029296
rs1029296
1 1.000 0.040 6 32888604 intergenic variant T/C snv 0.14 0.800 1.000 1 2013 2013
dbSNP: rs11969002
rs11969002
1 1.000 0.040 6 32891971 upstream gene variant G/A;T snv 0.800 1.000 1 2013 2013
dbSNP: rs1245582
rs1245582
1 1.000 0.040 10 72018509 downstream gene variant C/G;T snv 0.800 1.000 1 2013 2013
dbSNP: rs17034687
rs17034687
1 1.000 0.040 3 3638168 intergenic variant C/G;T snv 0.800 1.000 1 2013 2013
dbSNP: rs2187689
rs2187689
1 1.000 0.040 6 32884870 intergenic variant T/C snv 0.14 0.800 1.000 1 2013 2013
dbSNP: rs3749982
rs3749982
1 1.000 0.040 6 32894830 upstream gene variant T/A;G snv 0.800 1.000 1 2013 2013
dbSNP: rs4875102
rs4875102
1 1.000 0.040 8 4427170 intron variant G/A;T snv 0.800 1.000 1 2013 2013
dbSNP: rs6457690
rs6457690
1 1.000 0.040 6 32887940 intergenic variant G/A snv 0.14 0.800 1.000 1 2013 2013
dbSNP: rs6936004
rs6936004
1 1.000 0.040 6 32889157 intergenic variant T/C;G snv 0.800 1.000 1 2013 2013
dbSNP: rs7744666
rs7744666
1 1.000 0.040 6 32891935 upstream gene variant T/C snv 0.13 0.800 1.000 1 2013 2013
dbSNP: rs926849
rs926849
1 1.000 0.040 6 161740587 intron variant C/T snv 0.67 0.800 1.000 1 2013 2013
dbSNP: rs9301951
rs9301951
1 1.000 0.040 13 94300578 intron variant T/C;G snv 0.800 1.000 1 2013 2013
dbSNP: rs9469300
rs9469300
1 1.000 0.040 6 32892975 upstream gene variant G/A snv 0.13 0.800 1.000 1 2013 2013
dbSNP: rs10735810
rs10735810
VDR
26 0.662 0.640 12 47879112 start lost A/C;G;T snv 0.010 1.000 1 2017 2017
dbSNP: rs11076008
rs11076008
FTO
2 0.925 0.120 16 53893411 intron variant G/A;C snv 0.010 1.000 1 2013 2013
dbSNP: rs11200638
rs11200638
14 0.724 0.280 10 122461028 non coding transcript exon variant G/A snv 0.23 0.010 1.000 1 2010 2010
dbSNP: rs143383
rs143383
17 0.724 0.320 20 35438203 5 prime UTR variant G/A snv 0.47 0.010 1.000 1 2018 2018
dbSNP: rs16924573
rs16924573
1 1.000 0.040 10 24315964 intron variant G/A snv 8.8E-02 0.010 1.000 1 2011 2011
dbSNP: rs1793937
rs1793937
1 1.000 0.040 12 47981692 intron variant C/G snv 0.30 0.010 1.000 1 2017 2017
dbSNP: rs1793953
rs1793953
2 0.925 0.080 12 47999743 non coding transcript exon variant G/A snv 0.53 0.010 1.000 1 2017 2017
dbSNP: rs1799750
rs1799750
48 0.592 0.760 11 102799765 intron variant C/- delins 0.50 0.010 1.000 1 2013 2013