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: rs1023741
rs1023741
1 1.000 0.080 10 96663139 intron variant T/C snv 0.14 0.700 1.000 1 2019 2019
dbSNP: rs10920654
rs10920654
1 1.000 0.080 1 190162620 intron variant C/T snv 0.22 0.700 1.000 1 2019 2019
dbSNP: rs111861762
rs111861762
1 1.000 0.080 2 233672556 missense variant C/T snv 1.0E-04 3.8E-04 0.010 1.000 1 2014 2014
dbSNP: rs1145724
rs1145724
1 1.000 0.080 6 90477791 intergenic variant T/C snv 0.27 0.700 1.000 1 2019 2019
dbSNP: rs11574077
rs11574077
VDR
1 1.000 0.080 12 47859144 intron variant T/C snv 3.3E-02 0.010 1.000 1 2018 2018
dbSNP: rs11692570
rs11692570
1 1.000 0.080 2 6637860 non coding transcript exon variant C/T snv 0.16 0.700 1.000 1 2019 2019
dbSNP: rs12949587
rs12949587
1 1.000 0.080 17 79365094 intron variant C/T snv 0.13 0.700 1.000 1 2019 2019
dbSNP: rs13402783
rs13402783
1 1.000 0.080 2 85787998 3 prime UTR variant A/G snv 8.7E-02 0.700 1.000 1 2019 2019
dbSNP: rs1372330
rs1372330
1 1.000 0.080 9 116757309 intron variant G/A snv 0.13 0.700 1.000 1 2019 2019
dbSNP: rs1426107
rs1426107
1 1.000 0.080 4 14294676 regulatory region variant C/G;T snv 9.1E-02 0.700 1.000 1 2019 2019
dbSNP: rs17053011
rs17053011
1 1.000 0.080 5 155934106 intron variant G/T snv 0.13 0.700 1.000 1 2019 2019
dbSNP: rs17082301
rs17082301
1 1.000 0.080 4 53026989 intron variant G/A snv 0.16 0.700 1.000 1 2019 2019
dbSNP: rs17201864
rs17201864
1 1.000 0.080 15 88877743 3 prime UTR variant C/A;T snv 0.700 1.000 1 2019 2019
dbSNP: rs2163746
rs2163746
1 1.000 0.080 5 155918211 intron variant A/G snv 0.14 0.700 1.000 1 2019 2019
dbSNP: rs2327990
rs2327990
1 1.000 0.080 20 16208618 intron variant T/C snv 0.80 0.700 1.000 1 2019 2019
dbSNP: rs2366964
rs2366964
1 1.000 0.080 3 59944946 intron variant A/G snv 0.16 0.700 1.000 1 2019 2019
dbSNP: rs2936519
rs2936519
1 1.000 0.080 8 6781719 non coding transcript exon variant G/A snv 0.20 0.700 1.000 1 2015 2015
dbSNP: rs368295543
rs368295543
1 1.000 0.080 4 15778625 missense variant A/G snv 1.2E-05 2.1E-05 0.010 1.000 1 2014 2014
dbSNP: rs3861289
rs3861289
1 1.000 0.080 18 43111710 intron variant C/T snv 9.6E-02 0.700 1.000 1 2019 2019
dbSNP: rs4239258
rs4239258
1 1.000 0.080 17 7493724 intron variant A/G;T snv 0.700 1.000 1 2019 2019
dbSNP: rs4754687
rs4754687
1 1.000 0.080 11 100559322 intergenic variant A/C snv 0.75 0.700 1.000 1 2019 2019
dbSNP: rs5749032
rs5749032
1 1.000 0.080 22 17313079 intergenic variant A/G snv 0.37 0.700 1.000 1 2019 2019
dbSNP: rs6110524
rs6110524
1 1.000 0.080 20 15130492 intron variant A/G snv 0.88 0.700 1.000 1 2019 2019
dbSNP: rs7153665
rs7153665
YY1
1 1.000 0.080 14 100264583 intron variant A/G snv 0.63 0.700 1.000 1 2019 2019
dbSNP: rs756055
rs756055
1 1.000 0.080 14 100224841 intron variant A/G snv 0.34 0.700 1.000 1 2019 2019