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: rs1105358
rs1105358
1 1.000 0.080 9 16265821 intron variant G/C snv 0.10 0.700 1.000 1 2009 2009
dbSNP: rs11081843
rs11081843
1 1.000 0.080 18 34103632 intron variant T/C snv 0.16 0.700 1.000 1 2009 2009
dbSNP: rs11083572
rs11083572
1 1.000 0.080 19 28604968 intron variant T/A;C snv 0.700 1.000 1 2009 2009
dbSNP: rs11165851
rs11165851
1 1.000 0.080 1 97380021 intron variant T/A snv 0.93 0.700 1.000 1 2009 2009
dbSNP: rs11189017
rs11189017
1 1.000 0.080 10 81258621 intergenic variant T/G snv 1.0E-02 0.700 1.000 1 2009 2009
dbSNP: rs11206948
rs11206948
1 1.000 0.080 1 56984813 intron variant T/C snv 3.6E-02 0.700 1.000 1 2009 2009
dbSNP: rs11221067
rs11221067
1 1.000 0.080 11 127823799 intergenic variant C/T snv 8.8E-02 0.700 1.000 1 2009 2009
dbSNP: rs11238999
rs11238999
1 1.000 0.080 10 44345031 regulatory region variant G/A;C snv 0.700 1.000 1 2009 2009
dbSNP: rs11574049
rs11574049
VDR
1 1.000 0.080 12 47878732 intron variant A/G snv 1.6E-02 0.700 1.000 1 2009 2009
dbSNP: rs11604865
rs11604865
1 1.000 0.080 11 40636452 intron variant T/C snv 0.15 0.700 1.000 1 2009 2009
dbSNP: rs1163521
rs1163521
1 1.000 0.080 1 105786097 intergenic variant T/A;C;G snv 0.700 1.000 1 2009 2009
dbSNP: rs11687856
rs11687856
1 1.000 0.080 2 31117780 intron variant G/A snv 0.19 0.700 1.000 1 2009 2009
dbSNP: rs11697253
rs11697253
1 1.000 0.080 20 25014378 intron variant A/G snv 9.9E-02 0.700 1.000 1 2009 2009
dbSNP: rs11697653
rs11697653
1 1.000 0.080 20 43909379 regulatory region variant T/A;G snv 0.700 1.000 1 2009 2009
dbSNP: rs11774662
rs11774662
1 1.000 0.080 8 41279923 intron variant T/C snv 0.30 0.700 1.000 1 2009 2009
dbSNP: rs11853442
rs11853442
1 1.000 0.080 15 29850170 intron variant G/A;T snv 0.42 0.700 1.000 1 2009 2009
dbSNP: rs11963900
rs11963900
1 1.000 0.080 6 123895157 intron variant G/T snv 4.5E-02 0.700 1.000 1 2009 2009
dbSNP: rs1201324
rs1201324
1 1.000 0.080 13 89601725 intron variant A/G snv 0.98 0.700 1.000 1 2009 2009
dbSNP: rs1204803
rs1204803
1 1.000 0.080 6 116225703 intron variant G/A;T snv 0.700 1.000 1 2009 2009
dbSNP: rs1209710
rs1209710
1 1.000 0.080 3 138387856 intron variant C/T snv 0.82 0.700 1.000 1 2009 2009
dbSNP: rs12123414
rs12123414
1 1.000 0.080 1 79919071 intergenic variant G/A;C snv 0.34 0.700 1.000 1 2009 2009
dbSNP: rs12147450
rs12147450
1 1.000 0.080 14 20489274 intergenic variant T/C snv 0.17 0.700 1.000 1 2009 2009
dbSNP: rs12264969
rs12264969
1 1.000 0.080 10 3508421 intergenic variant T/C snv 0.13 0.700 1.000 1 2009 2009
dbSNP: rs12270184
rs12270184
1 1.000 0.080 11 102659700 intergenic variant C/T snv 8.5E-03 0.700 1.000 1 2009 2009
dbSNP: rs12273907
rs12273907
1 1.000 0.080 11 88519531 intron variant G/A snv 0.15 0.700 1.000 1 2009 2009