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: rs2294008
rs2294008
PSCA
15 0.724 0.179 8 142680513 5 prime UTR variant C/T snp 0.46 0.45 0.020 1.000 2 2013 2015
dbSNP: rs10434
rs10434
VEGFA
8 0.769 0.286 6 43785475 3 prime UTR variant A/G snp 0.59 0.010 1.000 1 2009 2009
dbSNP: rs1800470
rs1800470
TGFB1
46 0.596 0.643 19 41353016 missense variant G/A,C snp 0.55; 2.4E-04 0.60 0.010 1.000 1 2007 2007
dbSNP: rs25648
rs25648
VEGFA
9 0.769 0.357 6 43771240 synonymous variant C/G,T snp 8.5E-06; 0.16 0.14 0.010 < 0.001 1 2009 2009
dbSNP: rs3025039
rs3025039
VEGFA
28 0.638 0.536 6 43784799 3 prime UTR variant C/T snp 0.13 0.010 1.000 1 2009 2009
dbSNP: rs4880
rs4880
SOD2
81 0.536 0.643 6 159692840 missense variant A/G snp 0.48 0.47 0.010 1.000 1 2011 2011
dbSNP: rs5743618
rs5743618
TLR1
14 0.724 0.321 4 38797027 missense variant C/A snp 0.53 0.47 0.010 1.000 1 2013 2013