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: rs755622
rs755622
44 0.611 0.720 22 23894205 intron variant G/C snv 0.26 0.030 1.000 3 2012 2020
dbSNP: rs204989
rs204989
2 0.925 0.120 6 32194075 intron variant G/A snv 0.21 0.020 1.000 2 2016 2016
dbSNP: rs10036748
rs10036748
11 0.752 0.360 5 151078585 intron variant C/A;T snv 0.010 1.000 1 2019 2019
dbSNP: rs10491322
rs10491322
3 0.925 0.120 5 134194449 3 prime UTR variant A/G snv 9.5E-02 0.010 1.000 1 2018 2018
dbSNP: rs10499194
rs10499194
10 0.752 0.400 6 137681500 intron variant C/T snv 0.24 0.010 < 0.001 1 2010 2010
dbSNP: rs10911363
rs10911363
2 0.925 0.120 1 183580622 intron variant G/T snv 0.30 0.010 1.000 1 2011 2011
dbSNP: rs11168268
rs11168268
VDR
2 0.925 0.120 12 47858029 intron variant G/A snv 0.57 0.010 1.000 1 2013 2013
dbSNP: rs11747270
rs11747270
7 0.790 0.240 5 150879305 intron variant A/G snv 0.21 0.010 1.000 1 2020 2020
dbSNP: rs1194611372
rs1194611372
9 0.763 0.320 1 152032679 missense variant A/C snv 0.010 1.000 1 2014 2014
dbSNP: rs1234315
rs1234315
6 0.807 0.400 1 173209324 upstream gene variant C/T snv 0.57 0.010 1.000 1 2011 2011
dbSNP: rs13277113
rs13277113
BLK
18 0.695 0.520 8 11491677 intron variant G/A snv 0.25 0.010 1.000 1 2011 2011
dbSNP: rs1477353313
rs1477353313
ACR
2 0.925 0.120 22 50744085 missense variant T/G snv 0.010 1.000 1 2004 2004
dbSNP: rs1544410
rs1544410
VDR
78 0.542 0.760 12 47846052 intron variant C/A;G;T snv 0.010 1.000 1 2019 2019
dbSNP: rs1562444
rs1562444
2 0.925 0.120 11 92982683 3 prime UTR variant G/A snv 0.55 0.010 1.000 1 2019 2019
dbSNP: rs17197936
rs17197936
3 0.925 0.040 13 37601702 upstream gene variant T/C snv 5.2E-02 0.010 1.000 1 2014 2014
dbSNP: rs1800925
rs1800925
37 0.627 0.560 5 132657117 non coding transcript exon variant C/G;T snv 0.010 1.000 1 2011 2011
dbSNP: rs204991
rs204991
3 0.882 0.200 6 32193589 intron variant T/C snv 0.21 0.010 1.000 1 2016 2016
dbSNP: rs2165667
rs2165667
2 0.925 0.040 4 186540475 intron variant A/G;T snv 0.010 1.000 1 2019 2019
dbSNP: rs2234693
rs2234693
77 0.555 0.680 6 151842200 intron variant T/C snv 0.47 0.010 1.000 1 2017 2017
dbSNP: rs2248098
rs2248098
VDR
4 0.925 0.120 12 47859573 intron variant A/G;T snv 0.010 1.000 1 2013 2013
dbSNP: rs2670660
rs2670660
15 0.708 0.400 17 5615686 intron variant A/G snv 0.41 0.010 1.000 1 2012 2012
dbSNP: rs3024498
rs3024498
7 0.790 0.360 1 206768184 3 prime UTR variant T/C snv 0.20 0.010 1.000 1 2018 2018
dbSNP: rs35761398
rs35761398
19 0.701 0.520 1 23875429 missense variant TT/CC mnv 0.010 1.000 1 2018 2018
dbSNP: rs3890733
rs3890733
VDR
3 0.882 0.120 12 47895590 intron variant C/T snv 0.27 0.010 1.000 1 2013 2013
dbSNP: rs397507444
rs397507444
306 0.405 0.880 1 11794407 missense variant T/G snv 0.010 1.000 1 2018 2018