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: rs10455872
rs10455872
LPA
33 0.662 0.320 6 160589086 intron variant A/G snv 4.3E-02 0.820 1.000 2 2013 2019
dbSNP: rs6702619
rs6702619
LINC01708
4 0.851 0.200 1 99580690 intron variant T/G snv 0.35 0.700 1.000 1 2018 2018
dbSNP: rs1205
rs1205
CRP
46 0.602 0.680 1 159712443 3 prime UTR variant C/T snv 0.30 0.010 1.000 1 2015 2015
dbSNP: rs761508282
rs761508282
NOTCH1
2 1.000 0.080 9 136508288 missense variant G/C snv 8.1E-06 2.1E-05 0.010 1.000 1 2013 2013