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: rs121913364
rs121913364
25 0.652 0.429 7 140753334 missense variant T/C,G snp 4.0E-06 0.720 1.000 2 2012 2016
dbSNP: rs11554290
rs11554290
36 0.618 0.464 1 114713908 missense variant T/A,C,G snp 0.700 5 2003 2014
dbSNP: rs104894171
rs104894171
2 0.923 0.036 10 87508507 missense variant A/G snp 0.700 1 2001 2001
dbSNP: rs114817817
rs114817817
2 0.923 0.036 12 64108967 missense variant C/T snp 1.1E-03 5.1E-04 0.700 1 2013 2013
dbSNP: rs119486096
rs119486096
2 0.923 0.036 10 87505037 missense variant C/T snp 0.700 1 2001 2001
dbSNP: rs781626187
rs781626187
2 0.923 0.036 12 64016970 missense variant A/C,T snp 2.9E-05; 4.1E-06 0.700 1 2013 2013
dbSNP: rs797044990
rs797044990
2 0.923 0.036 12 64062938 missense variant G/A snp 0.700 1 2013 2013
dbSNP: rs28933406
rs28933406
24 0.667 0.429 11 533875 missense variant G/C,T snp 0.700 0
dbSNP: rs113488022
rs113488022
267 0.407 0.786 7 140753336 missense variant snp 4.0E-06 0.040 1.000 4 2007 2016
dbSNP: rs10735810
rs10735810
VDR
17 0.692 0.357 12 47879112 start lost snp 0.010 1.000 1 2009 2009
dbSNP: rs11214077
rs11214077
6 0.821 0.107 11 112087953 missense variant A/G snp 6.6E-03 4.8E-03 0.010 1.000 1 2015 2015
dbSNP: rs121908874
rs121908874
5 0.846 0.071 14 81143584 missense variant T/C snp 0.010 1.000 1 2005 2005
dbSNP: rs121913274
rs121913274
33 0.626 0.286 3 179218304 missense variant A/C,G,T snp 0.010 1.000 1 2012 2012
dbSNP: rs121913530
rs121913530
39 0.615 0.321 12 25245351 missense variant C/A,G,T snp 0.010 1.000 1 2006 2006
dbSNP: rs17849071
rs17849071
2 0.923 0.071 3 179218439 intron variant T/G snp 7.7E-02 0.010 1.000 1 2013 2013
dbSNP: rs1799939
rs1799939
RET
18 0.685 0.250 10 43114671 missense variant G/A,C snp 0.21 0.16 0.010 1.000 1 2016 2016
dbSNP: rs1800861
rs1800861
RET
3 0.878 0.143 10 43118395 missense variant G/A,T snp 0.74 0.78 0.010 1.000 1 2016 2016
dbSNP: rs1800863
rs1800863
RET
3 0.878 0.143 10 43120185 missense variant C/A,G snp 1.6E-05; 0.21 0.17 0.010 1.000 1 2016 2016
dbSNP: rs752021744
rs752021744
21 0.699 0.429 3 138759306 T/C snp 1.2E-05 0.010 1.000 1 2014 2014
dbSNP: rs7975232
rs7975232
VDR
26 0.652 0.500 12 47845054 intron variant C/A snp 0.51 0.54 0.010 1.000 1 2009 2009