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: rs76854597
rs76854597
ANO5
1 11 22200238 intron variant A/C;T snv 0.700 1.000 1 2018 2018
dbSNP: rs11624106
rs11624106
SAMD4A
1 14 54713435 intron variant A/G snv 0.16 0.700 1.000 1 2018 2018
dbSNP: rs11670986
rs11670986 		1 19 54270639 downstream gene variant A/G snv 8.8E-02 0.700 1.000 1 2018 2018
dbSNP: rs1279143
rs1279143
AKAP6
1 14 32705894 intron variant A/G snv 0.41 0.700 1.000 1 2018 2018
dbSNP: rs137933779
rs137933779
IQGAP3
1 1 156529759 intron variant A/G snv 7.1E-03 0.700 1.000 1 2018 2018
dbSNP: rs2361797
rs2361797
LILRB5
1 19 54249685 3 prime UTR variant A/G snv 0.54 0.700 1.000 1 2014 2014
dbSNP: rs7136716
rs7136716 		6 0.851 0.080 12 7538538 regulatory region variant A/G snv 0.22 0.700 1.000 1 2010 2010
dbSNP: rs9607721
rs9607721
MRTFA
1 22 40466116 intron variant A/G snv 0.18 0.700 1.000 1 2018 2018
dbSNP: rs2693560
rs2693560 		1 6 117202508 intergenic variant A/G;T snv 0.700 1.000 1 2018 2018
dbSNP: rs2819598
rs2819598 		1 6 117132241 intergenic variant A/G;T snv 0.700 1.000 1 2018 2018
dbSNP: rs12557126
rs12557126 		1 X 143602181 regulatory region variant C/A snv 0.25 0.700 1.000 1 2018 2018
dbSNP: rs11431
rs11431
SAMD4A
1 14 54788955 3 prime UTR variant C/A;G;T snv 1.2E-05; 0.53 0.700 1.000 1 2018 2018
dbSNP: rs4665988
rs4665988
C2orf16
1 2 27538569 intron variant C/A;T snv 0.700 1.000 1 2018 2018
dbSNP: rs61871700
rs61871700
CPN1
3 10 100068504 intron variant C/A;T snv 0.800 1.000 1 2013 2013
dbSNP: rs7487435
rs7487435 		1 12 7531072 intergenic variant C/A;T snv 0.700 1.000 1 2018 2018
dbSNP: rs13013209
rs13013209
NEB
1 2 151643935 missense variant C/G snv 0.42 0.35 0.700 1.000 1 2018 2018
dbSNP: rs1801690
rs1801690
APOH
6 0.925 0.120 17 66212167 missense variant C/G snv 4.8E-02 4.0E-02 0.700 1.000 1 2018 2018
dbSNP: rs210966
rs210966
ROS1
1 6 117303435 intron variant C/G snv 0.74 0.700 1.000 1 2018 2018
dbSNP: rs7208815
rs7208815 		1 17 40012462 non coding transcript exon variant C/G;T snv 0.700 1.000 1 2018 2018
dbSNP: rs78139700
rs78139700
BVES ; BVES-AS1
1 6 105135997 intron variant C/G;T snv 8.2E-04 0.700 1.000 1 2018 2018
dbSNP: rs10007186
rs10007186
LINC01094
2 4 78667891 intron variant C/T snv 0.65 0.700 1.000 1 2018 2018
dbSNP: rs61751507
rs61751507
CPN1
3 1.000 0.080 10 100069757 missense variant C/T snv 4.2E-02 3.4E-02 0.700 1.000 1 2018 2018
dbSNP: rs961183
rs961183
UBAP1
1 9 34243686 intron variant C/T snv 0.33 0.700 1.000 1 2018 2018
dbSNP: rs10162508
rs10162508 		1 14 35339056 intergenic variant G/A snv 0.38 0.700 1.000 1 2018 2018
dbSNP: rs11237485
rs11237485
GAB2
1 11 78414965 intron variant G/A snv 0.16 0.700 1.000 1 2018 2018