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: rs11239550
rs11239550
MARCHF8
3 10 45529281 intron variant A/G snv 0.31 0.800 1.000 1 2009 2009
dbSNP: rs1211375
rs1211375
LUC7L
4 1.000 0.040 16 190281 intron variant A/C;T snv 0.800 1.000 1 2013 2013
dbSNP: rs12718597
rs12718597
IKZF1
2 7 50360730 intron variant C/A;T snv 0.800 1.000 1 2009 2009
dbSNP: rs131794
rs131794
ODF3B
2 22 50533323 upstream gene variant A/C;G;T snv 0.800 1.000 1 2009 2009
dbSNP: rs2540917
rs2540917
MIR4432HG
3 2 60381624 intron variant T/C snv 0.29 0.800 1.000 1 2009 2009
dbSNP: rs4466998
rs4466998
FNTB ; MAX ; CHURC1-FNTB
2 14 65008822 intron variant C/A;G snv 0.800 1.000 1 2009 2009
dbSNP: rs5987027
rs5987027
MPP1
2 X 154785832 intron variant C/T snv 7.8E-02 0.800 1.000 1 2013 2013
dbSNP: rs7189020
rs7189020
FAM234A
2 16 254804 intron variant A/T snv 0.55 0.800 1.000 1 2009 2009
dbSNP: rs7786877
rs7786877 		3 7 100616392 downstream gene variant A/G snv 0.22 0.800 1.000 1 2009 2009
dbSNP: rs10107630
rs10107630
CCDC26
3 8 129591389 intron variant C/T snv 0.54 0.700 1.000 1 2016 2016
dbSNP: rs10164806
rs10164806
ZEB2
2 2 144435759 intron variant C/T snv 6.7E-02 0.700 1.000 1 2018 2018
dbSNP: rs10197140
rs10197140
ACOXL
3 2 110852366 intron variant T/C snv 0.28 0.700 1.000 1 2016 2016
dbSNP: rs10207392
rs10207392
ACOXL ; MIR4435-2HG
2 2 111092082 intron variant A/G snv 0.48 0.700 1.000 1 2012 2012
dbSNP: rs10225965
rs10225965
CDK6 ; LOC112268009
1 7 92644264 intron variant C/T snv 0.26 0.700 1.000 1 2016 2016
dbSNP: rs10267576
rs10267576
H2AZ2
1 7 44831334 intron variant T/C snv 0.35 0.700 1.000 1 2016 2016
dbSNP: rs10415135
rs10415135
ZBTB7A
3 19 4061546 intron variant C/T snv 0.23 0.700 1.000 1 2016 2016
dbSNP: rs10420951
rs10420951 		2 19 18526808 upstream gene variant C/G snv 0.81 0.700 1.000 1 2016 2016
dbSNP: rs1053004
rs1053004
STAT3
11 0.776 0.280 17 42314074 3 prime UTR variant G/A snv 0.48 0.700 1.000 1 2016 2016
dbSNP: rs10736831
rs10736831
TMEM72-AS1
3 10 44906863 intron variant G/A snv 0.55 0.700 1.000 1 2018 2018
dbSNP: rs10751450
rs10751450
ATP2B4
2 1 203681817 intron variant C/G;T snv 0.700 1.000 1 2016 2016
dbSNP: rs10758656
rs10758656
RCL1
7 9 4852599 intron variant A/G snv 0.19 0.700 1.000 1 2018 2018
dbSNP: rs10766533
rs10766533
CSRP3 ; CSRP3-AS1
4 11 19203130 intron variant T/A snv 0.62 0.700 1.000 1 2016 2016
dbSNP: rs10783487
rs10783487
ATG101
2 12 52068035 upstream gene variant G/A;T snv 0.700 1.000 1 2016 2016
dbSNP: rs10849023
rs10849023 		4 12 4223312 intergenic variant C/T snv 0.22 0.700 1.000 1 2017 2017
dbSNP: rs10923397
rs10923397 		2 1 117708521 regulatory region variant C/T snv 0.14 0.700 1.000 1 2016 2016