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: rs1061170
rs1061170
CFH
72 0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 0.010 1.000 1 2013 2013
dbSNP: rs4505848
rs4505848
KIAA1109
8 0.776 0.400 4 122211337 intron variant A/G snv 0.29 0.010 1.000 1 2012 2012
dbSNP: rs4936742
rs4936742
UBASH3B
2 0.925 0.200 11 122770378 intron variant T/C snv 0.64 0.010 1.000 1 2019 2019
dbSNP: rs7197
rs7197
HLA-DRA
3 0.882 0.200 6 32444803 3 prime UTR variant T/C;G snv 0.83 0.010 1.000 1 2017 2017
dbSNP: rs800292
rs800292
CFH
33 0.645 0.560 1 196673103 missense variant G/A snv 0.32 0.40 0.010 1.000 1 2012 2012