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: rs10859871
rs10859871 		2 1.000 0.040 12 95318100 intron variant A/C snv 0.37 0.850 1.000 5 2012 2017
dbSNP: rs1250248
rs1250248
FN1
4 1.000 0.040 2 215422370 intron variant A/G snv 0.77 0.030 1.000 3 2013 2019
dbSNP: rs2235529
rs2235529
WNT4
3 1.000 0.040 1 22123994 intron variant C/T snv 0.13 0.820 1.000 3 2013 2020
dbSNP: rs3820282
rs3820282
WNT4 ; LOC105376845
2 0.925 0.120 1 22141722 intron variant C/T snv 0.13 0.030 1.000 3 2015 2019
dbSNP: rs4141819
rs4141819
LOC105374786
2 1.000 0.040 2 67637543 intron variant C/T snv 0.71 0.820 1.000 3 2012 2015
dbSNP: rs10965235
rs10965235
CDKN2B-AS1
1 1.000 0.040 9 22115106 intron variant C/A snv 0.15 0.820 1.000 2 2010 2014
dbSNP: rs11674184
rs11674184
GREB1
1 1.000 0.040 2 11581409 intron variant T/A;G snv 0.710 0.500 2 2017 2019
dbSNP: rs3761549
rs3761549
FOXP3
18 0.724 0.480 X 49260888 intron variant G/A snv 9.6E-02 0.020 1.000 2 2011 2012
dbSNP: rs7582694
rs7582694
STAT4
9 0.763 0.400 2 191105394 intron variant C/G snv 0.77 0.020 1.000 2 2016 2019
dbSNP: rs7739264
rs7739264
LOC100506885
1 1.000 0.040 6 19785357 intron variant C/G;T snv 0.810 1.000 2 2012 2015
dbSNP: rs10129516
rs10129516
LOC105370531
1 1.000 0.040 14 63133372 intron variant T/A;C snv 0.710 < 0.001 1 2017 2017
dbSNP: rs10419023
rs10419023
GRIN2D
1 1.000 0.040 19 48427965 intron variant C/T snv 0.13 0.700 1.000 1 2017 2017
dbSNP: rs10757272
rs10757272
CDKN2B-AS1
6 0.851 0.160 9 22088261 intron variant C/T snv 0.41 0.700 1.000 1 2017 2017
dbSNP: rs10777670
rs10777670
FGD6
1 1.000 0.040 12 95181055 intron variant G/A snv 0.23 0.700 1.000 1 2012 2012
dbSNP: rs10835638
rs10835638
FSHB ; LOC105376607
2 0.925 0.080 11 30230805 intron variant G/A;T snv 0.010 1.000 1 2016 2016
dbSNP: rs10859856
rs10859856
VEZT
1 1.000 0.040 12 95237500 intron variant T/C snv 0.48 0.700 1.000 1 2012 2012
dbSNP: rs11031006
rs11031006
LOC105376607
8 0.882 0.120 11 30204981 intron variant G/A snv 0.11 0.010 1.000 1 2017 2017
dbSNP: rs11085835
rs11085835
CACNA1A
1 1.000 0.040 19 13221196 intron variant T/A;C snv 0.700 1.000 1 2017 2017
dbSNP: rs11592737
rs11592737
CYP2C19
2 0.925 0.040 10 94843657 intron variant A/G snv 0.21 0.010 1.000 1 2015 2015
dbSNP: rs1159327
rs1159327
ESR1
1 1.000 0.040 6 151726887 intron variant C/T snv 0.32 0.010 1.000 1 2013 2013
dbSNP: rs116175374
rs116175374
CAPN14
1 1.000 0.040 2 31202319 intron variant G/A snv 4.9E-02 0.700 1.000 1 2017 2017
dbSNP: rs11651755
rs11651755
HNF1B
9 0.763 0.160 17 37739849 intron variant T/C snv 0.52 0.010 1.000 1 2017 2017
dbSNP: rs11692361
rs11692361
MEIS1
1 1.000 0.040 2 66496567 intron variant C/G;T snv 0.700 1.000 1 2017 2017
dbSNP: rs11977660
rs11977660
EGFR
1 1.000 0.040 7 55094643 intron variant T/C snv 0.42 0.010 1.000 1 2019 2019
dbSNP: rs12030576
rs12030576 		2 1.000 0.040 1 115274600 intron variant G/C;T snv 0.010 1.000 1 2018 2018