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: rs10936599
rs10936599
MYNN
32 0.637 0.600 3 169774313 synonymous variant C/T snv 0.29 0.21 0.700 0
dbSNP: rs11125529
rs11125529
ACYP2
3 0.882 0.280 2 54248729 intron variant C/A;T snv 0.700 0
dbSNP: rs2735940
rs2735940
TERT
25 0.689 0.400 5 1296371 upstream gene variant A/G snv 0.49 0.700 0
dbSNP: rs2736100
rs2736100
TERT
83 0.550 0.880 5 1286401 3 prime UTR variant C/A snv 0.52 0.700 0
dbSNP: rs398652
rs398652 		10 0.752 0.240 14 56058851 intergenic variant G/A snv 0.24 0.700 0
dbSNP: rs755017
rs755017
ZBTB46
2 0.925 0.080 20 63790269 synonymous variant A/C;G snv 0.17 0.700 0
dbSNP: rs7675998
rs7675998 		5 0.827 0.360 4 163086668 intergenic variant A/G;T snv 0.700 0
dbSNP: rs1143627
rs1143627
IL1B
47 0.605 0.760 2 112836810 5 prime UTR variant G/A snv 0.56 0.010 1.000 1 2019 2019
dbSNP: rs1143634
rs1143634
IL1B
52 0.597 0.680 2 112832813 synonymous variant G/A snv 0.19 0.19 0.010 1.000 1 2019 2019
dbSNP: rs16944
rs16944
IL1B
92 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 0.010 1.000 1 2019 2019
dbSNP: rs1799964
rs1799964
LTA ; TNF ; LOC100287329
47 0.608 0.760 6 31574531 upstream gene variant T/C snv 0.19 0.010 1.000 1 2018 2018
dbSNP: rs2853550
rs2853550
IL1B
3 0.882 0.120 2 112829544 downstream gene variant A/G snv 0.83 0.010 1.000 1 2019 2019