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: rs10046
rs10046
CYP19A1 ; MIR4713HG
18 0.708 0.400 15 51210789 3 prime UTR variant G/A snv 0.45 0.43 0.030 0.667 3 2011 2016
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: rs10131751
rs10131751 		1 1.000 0.040 14 28212010 intergenic variant C/A snv 9.2E-02 0.700 1.000 1 2017 2017
dbSNP: rs10167914
rs10167914 		1 1.000 0.040 2 112805784 TF binding site variant A/G snv 0.31 0.700 1.000 1 2017 2017
dbSNP: rs10282436
rs10282436
LOC100506236
1 1.000 0.040 7 25833490 upstream gene variant G/T snv 0.19 0.700 1.000 1 2012 2012
dbSNP: rs1037189404
rs1037189404
MUC1
8 0.776 0.280 1 155187519 missense variant C/T snv 0.010 1.000 1 2010 2010
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: rs1042522
rs1042522
TP53
242 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 0.060 0.833 6 2007 2016
dbSNP: rs1048943
rs1048943
CYP1A1
88 0.533 0.720 15 74720644 missense variant T/A;C;G snv 0.11 5.9E-02 0.020 1.000 2 2007 2016
dbSNP: rs10508881
rs10508881 		1 1.000 0.040 10 44046117 regulatory region variant A/G snv 0.50 0.800 1.000 1 2013 2013
dbSNP: rs1052133
rs1052133
OGG1 ; CAMK1
147 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 0.010 1.000 1 2010 2010
dbSNP: rs1055144
rs1055144
LOC100506236
3 1.000 0.040 7 25831489 non coding transcript exon variant C/T snv 0.16 0.700 1.000 1 2012 2012
dbSNP: rs1056836
rs1056836
CYP1B1
58 0.581 0.680 2 38071060 missense variant G/C snv 0.51 0.010 < 0.001 1 2007 2007
dbSNP: rs1065780
rs1065780
IGFBP1
1 1.000 0.040 7 45888078 upstream gene variant G/A snv 0.39 0.010 1.000 1 2012 2012
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: rs10794288
rs10794288
MUC2
1 1.000 0.040 11 1086825 non coding transcript exon variant C/G;T snv 0.010 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: rs10859871
rs10859871 		2 1.000 0.040 12 95318100 intron variant A/C snv 0.37 0.850 1.000 5 2012 2017
dbSNP: rs10895068
rs10895068
PGR ; PGR-AS1
14 0.752 0.240 11 101129483 5 prime UTR variant C/T snv 3.6E-02 0.010 1.000 1 2011 2011
dbSNP: rs10902088
rs10902088
MUC2
2 1.000 0.040 11 1090036 non coding transcript exon variant T/C snv 0.73 0.010 1.000 1 2012 2012
dbSNP: rs10917151
rs10917151
CDC42
3 0.925 0.040 1 22096228 3 prime UTR variant G/A snv 0.14 0.800 1.000 1 2013 2013
dbSNP: rs10953316
rs10953316
MUC17
1 1.000 0.040 7 101038481 synonymous variant A/C;G;T snv 8.0E-06; 0.64 0.010 1.000 1 2015 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