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: rs16986953
rs16986953 		1 1.000 0.040 2 19742712 intergenic variant G/A snv 0.11 0.800 1.000 5 2013 2018
dbSNP: rs7500448
rs7500448
CDH13
3 1.000 0.040 16 83012185 intron variant A/G snv 0.20 0.700 1.000 4 2017 2018
dbSNP: rs10840293
rs10840293
SWAP70
2 1.000 0.040 11 9729649 intron variant G/A;C snv 0.700 1.000 3 2015 2018
dbSNP: rs10857147
rs10857147 		9 1.000 0.040 4 80259918 intergenic variant A/T snv 0.25 0.700 1.000 3 2017 2018
dbSNP: rs11057830
rs11057830
SCARB1
5 0.851 0.040 12 124822507 intron variant G/A snv 0.15 0.710 1.000 3 2017 2019
dbSNP: rs11617955
rs11617955
COL4A1
1 1.000 0.040 13 110165755 intron variant T/A snv 9.3E-02 0.800 1.000 3 2013 2018
dbSNP: rs12493885
rs12493885
ARHGEF26 ; ARHGEF26-AS1
1 1.000 0.040 3 154122077 missense variant G/C snv 0.91 0.91 0.700 1.000 3 2017 2018
dbSNP: rs12740374
rs12740374
CELSR2
16 0.851 0.040 1 109274968 3 prime UTR variant G/T snv 0.22 0.710 1.000 3 2018 2018
dbSNP: rs17678683
rs17678683
LINC01412
1 1.000 0.040 2 144528992 intron variant T/G snv 7.2E-02 0.700 1.000 3 2015 2018
dbSNP: rs2487928
rs2487928
JCAD
1 1.000 0.040 10 30034963 intron variant G/A snv 0.34 0.710 1.000 3 2015 2018
dbSNP: rs3890011
rs3890011
CYP4A11
3 0.925 0.040 1 46933071 intron variant G/C snv 0.71 0.65 0.030 1.000 3 2013 2018
dbSNP: rs4888378
rs4888378
CFDP1
4 0.851 0.040 16 75298143 intron variant A/G snv 0.52 0.720 1.000 3 2012 2018
dbSNP: rs55730499
rs55730499
LPA
2 1.000 0.040 6 160584578 intron variant C/T snv 4.5E-02 0.700 1.000 3 2015 2018
dbSNP: rs7623687
rs7623687
RHOA ; TCTA
1 1.000 0.040 3 49411133 intron variant A/C;T snv 0.700 1.000 3 2017 2018
dbSNP: rs7678555
rs7678555 		1 1.000 0.040 4 119988346 intergenic variant A/C snv 0.23 0.700 1.000 3 2017 2018
dbSNP: rs8042271
rs8042271 		3 0.882 0.040 15 89030987 intergenic variant G/A;T snv 0.710 1.000 3 2015 2019
dbSNP: rs10139550
rs10139550
HHIPL1
1 1.000 0.040 14 99679373 3 prime UTR variant C/G snv 0.39 0.700 1.000 2 2015 2017
dbSNP: rs10755578
rs10755578
LPA
2 0.925 0.040 6 160548706 intron variant C/G snv 0.44 0.42 0.710 1.000 2 2009 2012
dbSNP: rs10841443
rs10841443
LINC02398
1 1.000 0.040 12 20067099 intron variant C/G snv 0.56 0.700 1.000 2 2017 2018
dbSNP: rs11057401
rs11057401
CCDC92
2 0.925 0.040 12 123942759 missense variant T/A snv 0.27 0.30 0.700 1.000 2 2017 2018
dbSNP: rs111245230
rs111245230
SVEP1
3 1.000 0.040 9 110407495 missense variant T/C snv 2.6E-02 2.3E-02 0.700 1.000 2 2017 2018
dbSNP: rs11170820
rs11170820
FLJ12825
1 1.000 0.040 12 54120131 non coding transcript exon variant C/A;G snv 0.700 1.000 2 2018 2018
dbSNP: rs11191416
rs11191416
LOC107984264
1 1.000 0.040 10 102845159 intron variant T/G snv 0.10 0.700 1.000 2 2015 2017
dbSNP: rs11810571
rs11810571
TDRKH ; TDRKH-AS1
1 1.000 0.040 1 151789832 intron variant C/A;G snv 0.700 1.000 2 2017 2018
dbSNP: rs12202017
rs12202017
LINC01312 ; TARID
1 1.000 0.040 6 133852013 intron variant A/C;G snv 0.30 0.700 1.000 2 2015 2017