Source: ALL
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: rs1466535
rs1466535
LRP1
9 0.790 0.160 12 57140687 intron variant G/A;C snv 0.010 1.000 1 2013 2013
dbSNP: rs1492099
rs1492099
AGTR1
5 0.882 0.120 3 148719716 intron variant T/A;C snv 0.89 0.010 1.000 1 2016 2016
dbSNP: rs1498373
rs1498373
DDAH1
4 0.882 0.120 1 85324950 intron variant G/A snv 0.28 0.010 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 2018 2018
dbSNP: rs233112
rs233112
DDAH1
3 0.925 0.040 1 85320068 3 prime UTR variant T/C snv 0.37 0.010 1.000 1 2019 2019
dbSNP: rs275653
rs275653
AGTR1
5 0.882 0.120 3 148697758 upstream gene variant A/G snv 0.20 0.010 1.000 1 2016 2016
dbSNP: rs731236
rs731236
VDR
81 0.542 0.760 12 47844974 synonymous variant A/G snv 0.33 0.34 0.010 1.000 1 2018 2018
dbSNP: rs7975232
rs7975232
VDR
56 0.576 0.760 12 47845054 intron variant C/A snv 0.51 0.55 0.010 1.000 1 2018 2018