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: rs11244787
rs11244787
ADAM12
2 1.000 0.080 10 126046147 intron variant A/G snv 0.13 0.13 0.010 1.000 1 2016 2016
dbSNP: rs17859821
rs17859821
MMP2
2 1.000 0.040 16 55478141 intron variant G/A;C snv 0.11 0.010 1.000 1 2016 2016
dbSNP: rs1871054
rs1871054
ADAM12
3 0.925 0.040 10 126093840 intron variant C/A;T snv 0.010 1.000 1 2016 2016
dbSNP: rs2285053
rs2285053
MMP2
15 0.752 0.320 16 55478465 intron variant C/T snv 0.12 0.010 1.000 1 2016 2016
dbSNP: rs243864
rs243864
MMP2
3 0.925 0.080 16 55478410 intron variant T/G snv 0.19 0.010 1.000 1 2016 2016
dbSNP: rs243866
rs243866
MMP2
8 0.827 0.120 16 55477625 intron variant G/A snv 0.19 0.010 1.000 1 2016 2016
dbSNP: rs5743708
rs5743708
TLR2
98 0.525 0.800 4 153705165 missense variant G/A snv 1.7E-02 1.8E-02 0.010 1.000 1 2017 2017