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: rs1800890
rs1800890
IL19
29 0.658 0.400 1 206776020 intron variant A/T snv 0.32 0.020 1.000 2 2007 2009
dbSNP: rs3769821
rs3769821
CASP8
4 0.851 0.200 2 201258707 intron variant C/T snv 0.57 0.020 1.000 2 2011 2013
dbSNP: rs10165970
rs10165970
NPAS2
18 0.708 0.320 2 100840527 intron variant G/A snv 0.16 0.010 1.000 1 2017 2017
dbSNP: rs10519097
rs10519097
RORA
18 0.708 0.320 15 60997989 intron variant C/T snv 0.13 0.010 1.000 1 2017 2017
dbSNP: rs11038689
rs11038689
CRY2
3 0.882 0.160 11 45852713 intron variant A/G snv 0.19 0.010 1.000 1 2009 2009
dbSNP: rs113686495
rs113686495
CASP8
4 0.925 0.160 2 201258757 intron variant ATTCTGTC/- delins 0.010 1.000 1 2011 2011
dbSNP: rs11943456
rs11943456
TMEM165
18 0.708 0.320 4 55410167 intron variant T/C snv 0.42 0.010 1.000 1 2017 2017
dbSNP: rs12203592
rs12203592
IRF4
38 0.649 0.320 6 396321 intron variant C/T snv 0.10 0.010 1.000 1 2009 2009
dbSNP: rs13178127
rs13178127
XRCC4
1 1.000 0.120 5 83293613 intron variant A/G snv 3.3E-02 0.010 1.000 1 2010 2010
dbSNP: rs1401417
rs1401417
CRY2
3 0.882 0.160 11 45858559 intron variant C/G snv 0.19 0.010 1.000 1 2009 2009
dbSNP: rs16994592
rs16994592
CD70
1 1.000 0.120 19 6586487 intron variant T/C snv 9.4E-02 0.010 1.000 1 2009 2009
dbSNP: rs17024869
rs17024869
NPAS2
18 0.708 0.320 2 100843581 intron variant T/C snv 8.3E-02 0.010 1.000 1 2017 2017
dbSNP: rs1785882
rs1785882
CARD16 ; LOC107984381
1 1.000 0.120 11 105052348 intron variant A/T snv 0.45 0.010 1.000 1 2009 2009
dbSNP: rs1800795
rs1800795
IL6 ; STEAP1B ; IL6-AS1
140 0.494 0.840 7 22727026 intron variant C/G snv 0.71 0.010 1.000 1 2015 2015
dbSNP: rs1800893
rs1800893
IL10 ; IL19
1 1.000 0.120 1 206773822 intron variant C/T snv 0.41 0.010 1.000 1 2017 2017
dbSNP: rs1800896
rs1800896
IL10 ; IL19
113 0.507 0.800 1 206773552 intron variant T/C snv 0.41 0.010 1.000 1 2015 2015
dbSNP: rs1921310
rs1921310
TANK
1 1.000 0.120 2 161192690 intron variant A/G snv 0.15 0.010 1.000 1 2009 2009
dbSNP: rs2069812
rs2069812
IL5
5 0.851 0.240 5 132544224 intron variant A/G snv 0.54 0.010 1.000 1 2011 2011
dbSNP: rs2071286
rs2071286
NOTCH4
12 0.752 0.280 6 32212119 intron variant C/T snv 0.17 0.010 1.000 1 2017 2017
dbSNP: rs207186
rs207186 		2 0.925 0.120 1 55359252 intron variant C/T snv 7.7E-03 0.010 1.000 1 2017 2017
dbSNP: rs2237060
rs2237060
RAD50 ; TH2LCRR
1 1.000 0.120 5 132635193 intron variant T/G snv 0.29 0.010 1.000 1 2010 2010
dbSNP: rs227060
rs227060
ATM ; C11orf65
3 0.882 0.160 11 108334154 intron variant C/T snv 0.27 0.010 1.000 1 2014 2014
dbSNP: rs2582869
rs2582869
TNFSF13B
1 1.000 0.120 13 108259797 intron variant A/G;T snv 0.010 1.000 1 2009 2009
dbSNP: rs2637988
rs2637988
IL1RN
1 1.000 0.120 2 113119202 intron variant G/A snv 0.53 0.010 1.000 1 2011 2011
dbSNP: rs2855429
rs2855429
COL11A2
2 0.925 0.120 6 33190412 intron variant A/C snv 0.78 0.010 1.000 1 2011 2011