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: rs3791679
rs3791679
EFEMP1 ; LOC112268416
11 0.925 0.120 2 55869757 intron variant A/G snv 0.20 0.700 1.000 7 2008 2019
dbSNP: rs2284746
rs2284746
MFAP2
6 1 16980180 intron variant C/A;G snv 0.700 1.000 6 2010 2019
dbSNP: rs3791675
rs3791675
EFEMP1
4 1.000 0.040 2 55884174 intron variant C/T snv 0.20 0.700 1.000 6 2008 2019
dbSNP: rs2093210
rs2093210
C14orf39
4 1.000 0.040 14 60490561 intron variant C/T snv 0.45 0.700 1.000 5 2010 2019
dbSNP: rs4369779
rs4369779
CABLES1
1 18 23155444 intron variant T/A;C snv 0.700 1.000 5 2014 2019
dbSNP: rs606452
rs606452
SERPINH1
4 1.000 0.040 11 75565133 intron variant A/C snv 0.78 0.700 1.000 5 2012 2019
dbSNP: rs7466269
rs7466269
FUBP3
3 9 130588697 intron variant A/G snv 0.33 0.700 1.000 5 2008 2017
dbSNP: rs1490384
rs1490384 		4 6 126530014 intron variant C/G;T snv 0.700 1.000 4 2010 2019
dbSNP: rs1812175
rs1812175
HHIP ; HHIP-AS1
6 4 144653692 intron variant A/G snv 0.79 0.700 1.000 4 2008 2019
dbSNP: rs2280470
rs2280470
ACAN
3 15 88852395 intron variant A/G snv 0.68 0.700 1.000 4 2010 2017
dbSNP: rs2871865
rs2871865
IGF1R ; IRAIN
2 15 98651667 intron variant C/G snv 0.21 0.700 1.000 4 2010 2019
dbSNP: rs4282339
rs4282339
SLIT3
2 5 168829235 intron variant G/A snv 0.18 0.700 1.000 4 2010 2019
dbSNP: rs6060369
rs6060369
UQCC1
2 20 35319358 intron variant T/C snv 0.49 0.700 1.000 4 2008 2019
dbSNP: rs6570507
rs6570507
ADGRG6
13 0.827 0.240 6 142358435 intron variant G/A snv 0.47 0.700 1.000 4 2009 2019
dbSNP: rs6763931
rs6763931
ZBTB38
4 0.925 0.080 3 141383991 intron variant G/A snv 0.54 0.700 1.000 4 2008 2019
dbSNP: rs6918981
rs6918981 		2 6 34270737 intron variant G/A snv 0.69 0.700 1.000 4 2009 2019
dbSNP: rs10906982
rs10906982
ADAMTSL3
2 15 83899406 intron variant T/A snv 0.63 0.700 1.000 3 2008 2019
dbSNP: rs10958476
rs10958476
PLAG1
2 8 56183249 intron variant T/C snv 0.16 0.700 1.000 3 2008 2014
dbSNP: rs11144688
rs11144688
PCSK5
2 9 75927370 intron variant G/A snv 9.2E-02 0.700 1.000 3 2010 2014
dbSNP: rs11658329
rs11658329
MAP3K3 ; STRADA ; LOC101927898
2 17 63685671 intron variant G/C snv 0.39 0.700 1.000 3 2011 2019
dbSNP: rs1415701
rs1415701
L3MBTL3
3 6 130024690 intron variant G/A snv 0.31 0.700 1.000 3 2013 2019
dbSNP: rs17511102
rs17511102
CDC42EP3 ; LOC105374465
3 2 37733470 intron variant A/G;T snv 0.700 1.000 3 2010 2019
dbSNP: rs1787200
rs1787200
DYM
2 18 49061284 intron variant G/A snv 0.71 0.700 1.000 3 2011 2019
dbSNP: rs1991431
rs1991431
ZBTB38
4 3 141414608 intron variant G/A snv 0.50 0.700 1.000 3 2013 2019
dbSNP: rs2282978
rs2282978
CDK6 ; LOC112268009
5 7 92635096 intron variant T/C snv 0.38 0.700 1.000 3 2008 2009