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: rs6846071
rs6846071
BANK1
2 4 101481058 intron variant T/G snv 0.15 0.700 1.000 1 2013 2013
dbSNP: rs6951245
rs6951245
C7orf50
2 7 1018557 intron variant G/A snv 0.12 0.700 1.000 1 2016 2016
dbSNP: rs771767
rs771767 		2 1.000 0.080 3 102029794 regulatory region variant A/G snv 0.70 0.700 1.000 1 2016 2016
dbSNP: rs9284725
rs9284725
IL1R1
1 2 102128394 intron variant C/A;T snv 0.82 0.700 1.000 1 2018 2018
dbSNP: rs4141632
rs4141632
IL1R1
1 2 102140679 intron variant A/G;T snv 0.700 1.000 1 2018 2018
dbSNP: rs10745954
rs10745954
C12orf42
1 12 103089316 intron variant A/G snv 0.60 0.800 1.000 2 2011 2019
dbSNP: rs10778213
rs10778213
C12orf42
1 12 103101373 intron variant T/C snv 0.57 0.800 1.000 1 2008 2008
dbSNP: rs4764725
rs4764725
C12orf42
1 12 103118536 intron variant T/C snv 0.56 0.700 1.000 1 2018 2018
dbSNP: rs10778215
rs10778215
C12orf42
2 12 103143488 intron variant T/A;G snv 0.700 1.000 1 2018 2018
dbSNP: rs1529711
rs1529711
CARM1
4 1.000 0.080 19 10912758 intron variant C/T snv 0.13 0.700 1.000 1 2016 2016
dbSNP: rs629301
rs629301
CELSR2
22 0.851 0.120 1 109275684 3 prime UTR variant G/T snv 0.74 0.700 1.000 1 2016 2016
dbSNP: rs646776
rs646776
CELSR2
25 0.752 0.240 1 109275908 downstream gene variant C/T snv 0.74 0.700 1.000 1 2016 2016
dbSNP: rs10744775
rs10744775
BRAP
2 12 111658411 intron variant T/C snv 0.44 0.700 1.000 1 2016 2016
dbSNP: rs10255299
rs10255299
DOCK4
2 7 111887504 intron variant G/A snv 0.11 0.700 1.000 1 2013 2013
dbSNP: rs5744256
rs5744256
IL18
6 0.827 0.120 11 112152125 intron variant A/G snv 0.16 0.700 1.000 1 2014 2014
dbSNP: rs1834481
rs1834481
IL18
5 0.882 0.160 11 112153104 non coding transcript exon variant C/G snv 0.16 0.700 1.000 1 2014 2014
dbSNP: rs5744222
rs5744222
TEX12 ; LOC107987164
1 11 112166291 intron variant G/A;T snv 0.700 1.000 1 2014 2014
dbSNP: rs7131094
rs7131094
BCO2
1 11 112174194 intron variant C/T snv 0.17 0.700 1.000 1 2014 2014
dbSNP: rs10891343
rs10891343
BCO2
2 11 112209661 intron variant T/C snv 0.44 0.700 1.000 1 2014 2014
dbSNP: rs2250417
rs2250417
BCO2
5 1.000 0.080 11 112214593 intron variant T/C snv 0.44 0.700 1.000 1 2014 2014
dbSNP: rs2285810
rs2285810
HECTD4
2 12 112261736 non coding transcript exon variant T/C snv 0.45 0.700 1.000 1 2016 2016
dbSNP: rs6761276
rs6761276
IL1F10
2 2 113074735 missense variant T/C snv 0.56 0.57 0.700 1.000 1 2014 2014
dbSNP: rs6743376
rs6743376
IL1F10
2 2 113074756 missense variant C/A snv 0.69 0.69 0.700 1.000 1 2014 2014
dbSNP: rs13386602
rs13386602 		1 2 113077243 downstream gene variant A/C snv 0.56 0.700 1.000 1 2014 2014
dbSNP: rs11678375
rs11678375 		1 2 113078114 downstream gene variant T/C snv 0.56 0.700 1.000 1 2014 2014