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: rs713993049
rs713993049
2 0.925 0.080 3 101232784 missense variant C/A snv 8.0E-06 0.010 1.000 1 2017 2017
dbSNP: rs16863247
rs16863247
2 0.925 0.160 1 162535706 regulatory region variant A/G snv 4.8E-02 0.010 1.000 1 2016 2016
dbSNP: rs6717924
rs6717924
2 0.925 0.160 2 202381581 intron variant G/A snv 0.13 0.010 1.000 1 2016 2016
dbSNP: rs699
rs699
AGT
134 0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 0.010 1.000 1 2011 2011
dbSNP: rs6354
rs6354
16 0.732 0.280 17 30222880 5 prime UTR variant G/C;T snv 0.010 1.000 1 2016 2016
dbSNP: rs61755797
rs61755797
3 0.882 0.080 6 42704565 missense variant G/A;C snv 4.0E-06 0.700 1.000 1 2019 2019
dbSNP: rs2228570
rs2228570
VDR
99 0.521 0.760 12 47879112 start lost A/C;G;T snv 0.63 0.010 1.000 1 2017 2017
dbSNP: rs11169953
rs11169953
1 1.000 0.080 12 51910615 intron variant C/T snv 0.36 0.010 1.000 1 2016 2016
dbSNP: rs706816
rs706816
1 1.000 0.080 12 51919180 missense variant A/G snv 0.26 0.31 0.010 1.000 1 2016 2016
dbSNP: rs8050136
rs8050136
FTO
32 0.716 0.560 16 53782363 intron variant C/A snv 0.40 0.010 1.000 1 2013 2013
dbSNP: rs28940275
rs28940275
1 1.000 0.080 11 61951822 missense variant A/C snv 0.800 1.000 19 1998 2012
dbSNP: rs281865204
rs281865204
1 1.000 0.080 11 61951823 missense variant C/G snv 0.700 1.000 18 1998 2011
dbSNP: rs199508634
rs199508634
1 1.000 0.080 11 61951826 missense variant G/A snv 2.8E-05 1.4E-05 0.010 1.000 1 2015 2015
dbSNP: rs28940276
rs28940276
1 1.000 0.080 11 61951831 missense variant G/A snv 0.800 1.000 19 1998 2012
dbSNP: rs281865205
rs281865205
1 1.000 0.080 11 61951832 missense variant T/C;G snv 0.800 1.000 19 1998 2012
dbSNP: rs281865206
rs281865206
1 1.000 0.080 11 61951834 missense variant G/A snv 0.700 1.000 18 1998 2011
dbSNP: rs281865207
rs281865207
2 1.000 0.080 11 61951835 missense variant C/T snv 0.700 1.000 18 1998 2011
dbSNP: rs281865208
rs281865208
1 1.000 0.080 11 61951838 missense variant A/G;T snv 4.0E-06 0.700 1.000 18 1998 2011
dbSNP: rs281865209
rs281865209
1 1.000 0.080 11 61951844 missense variant G/A;C snv 1.2E-05 0.700 1.000 18 1998 2011
dbSNP: rs281865210
rs281865210
1 1.000 0.080 11 61951853 missense variant C/T snv 0.700 1.000 18 1998 2011
dbSNP: rs281865211
rs281865211
1 1.000 0.080 11 61951856 missense variant T/G snv 0.700 1.000 18 1998 2011
dbSNP: rs281865212
rs281865212
1 1.000 0.080 11 61951867 missense variant C/G snv 0.700 1.000 18 1998 2011
dbSNP: rs281865213
rs281865213
1 1.000 0.080 11 61951878 stop gained G/A;T snv 4.0E-06 0.700 1.000 18 1998 2011
dbSNP: rs281865214
rs281865214
1 1.000 0.080 11 61951879 missense variant C/A;G;T snv 3.2E-05; 4.0E-06; 4.0E-06 0.710 1.000 19 1998 2012
dbSNP: rs281865215
rs281865215
1 1.000 0.080 11 61951880 missense variant G/A snv 1.4E-05 0.700 1.000 18 1998 2011