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: rs3802842
rs3802842
COLCA2 ; COLCA1
25 0.695 0.280 11 111300984 intron variant C/A snv 0.71 0.020 1.000 2 2010 2010
dbSNP: rs4939827
rs4939827
SMAD7
25 0.708 0.160 18 48927093 intron variant T/A;C snv 0.020 1.000 2 2012 2016
dbSNP: rs10484879
rs10484879
IL17A
5 0.827 0.160 6 52187159 intron variant G/A;T snv 0.010 1.000 1 2019 2019
dbSNP: rs10857561
rs10857561
MAPK8
1 1.000 0.080 10 48400595 intron variant G/A snv 0.29 0.010 1.000 1 2012 2012
dbSNP: rs10889675
rs10889675
IL23R
2 1.000 0.080 1 67256533 intron variant C/A snv 0.11 0.010 1.000 1 2012 2012
dbSNP: rs11247735
rs11247735
SELENON
1 1.000 0.080 1 25804968 intron variant G/A;C snv 0.010 1.000 1 2012 2012
dbSNP: rs11568820
rs11568820
VDR
27 0.672 0.480 12 47908762 intron variant C/T snv 0.38 0.010 1.000 1 2007 2007
dbSNP: rs11718498
rs11718498
TXNRD3
1 1.000 0.080 3 126654076 intron variant G/A snv 0.36 0.010 1.000 1 2012 2012
dbSNP: rs11721827
rs11721827
TLR3
4 0.851 0.200 4 186069983 intron variant A/C snv 0.12 0.010 1.000 1 2012 2012
dbSNP: rs12733285
rs12733285
ADIPOR1
12 0.776 0.120 1 202952912 intron variant C/T snv 0.26 0.010 1.000 1 2011 2011
dbSNP: rs1342387
rs1342387
ADIPOR1
12 0.776 0.120 1 202945228 intron variant T/C snv 0.53 0.010 1.000 1 2011 2011
dbSNP: rs17026425
rs17026425
IQCM
4 0.882 0.080 4 149751362 intron variant G/A snv 4.9E-02 0.700 1.000 1 2015 2015
dbSNP: rs17268122
rs17268122
ABCC4
2 1.000 0.080 13 95192240 intron variant G/A;C;T snv 0.010 1.000 1 2017 2017
dbSNP: rs1800469
rs1800469
TGFB1 ; B9D2
78 0.547 0.760 19 41354391 intron variant A/G snv 0.69 0.010 1.000 1 2011 2011
dbSNP: rs187115
rs187115
CD44
22 0.695 0.320 11 35154612 intron variant T/C snv 0.37 0.010 1.000 1 2019 2019
dbSNP: rs1970764
rs1970764
PPP1R13L
4 0.851 0.120 19 45387615 intron variant T/C snv 0.27 0.010 1.000 1 2013 2013
dbSNP: rs2072749
rs2072749
SELENON
1 1.000 0.080 1 25804530 intron variant T/C snv 0.23 0.010 1.000 1 2012 2012
dbSNP: rs2073438
rs2073438
ALOX12 ; ALOX12-AS1
2 0.925 0.160 17 6996757 intron variant G/A snv 0.20 0.010 1.000 1 2013 2013
dbSNP: rs2189517
rs2189517
RAD51B
3 0.882 0.080 14 68536271 intron variant A/G snv 0.49 0.010 1.000 1 2020 2020
dbSNP: rs2619112
rs2619112
ALOX15
3 0.882 0.160 17 4632090 intron variant A/C;G snv 4.0E-06; 0.53 0.010 1.000 1 2013 2013
dbSNP: rs2632159
rs2632159
PCAT1 ; LOC105375751
3 0.882 0.080 8 127021159 intron variant G/A;T snv 0.010 1.000 1 2019 2019
dbSNP: rs2705535
rs2705535
BTLA
1 1.000 0.080 3 112490080 intron variant C/T snv 8.4E-02 0.010 1.000 1 2015 2015
dbSNP: rs322351
rs322351
DUSP1
3 0.925 0.160 5 172767870 intron variant C/T snv 0.37 0.010 1.000 1 2012 2012
dbSNP: rs3804513
rs3804513
IL17A
4 0.851 0.080 6 52188399 intron variant A/T snv 2.4E-02 0.010 1.000 1 2019 2019
dbSNP: rs4659382
rs4659382
SELENON
1 1.000 0.080 1 25808435 intron variant C/A;G snv 0.010 1.000 1 2012 2012