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: rs10004195
rs10004195
TLR10
8 0.790 0.320 4 38783103 upstream gene variant T/A snv 0.29 0.010 1.000 1 2015 2015
dbSNP: rs10022537
rs10022537
PROM1
2 0.925 0.080 4 16075214 intron variant A/T snv 0.70 0.010 1.000 1 2015 2015
dbSNP: rs1002765
rs1002765
CHMP2B ; MIR4795
4 0.851 0.080 3 87227912 intron variant G/A;C snv 0.020 1.000 2 2016 2017
dbSNP: rs10029005
rs10029005
LINC02516
1 1.000 0.080 4 124530209 intron variant G/A snv 0.40 0.700 1.000 1 2020 2020
dbSNP: rs10036748
rs10036748
TNIP1
11 0.752 0.360 5 151078585 intron variant C/A;T snv 0.010 1.000 1 2016 2016
dbSNP: rs10052016
rs10052016
SLC6A3
2 0.925 0.080 5 1427996 intron variant A/G snv 0.22 0.010 1.000 1 2013 2013
dbSNP: rs10052657
rs10052657
PDE4D
7 0.807 0.120 5 59111944 intron variant C/A snv 0.17 0.010 1.000 1 2018 2018
dbSNP: rs10074991
rs10074991
PRKAA1
7 0.851 0.120 5 40790449 intron variant G/A snv 0.31 0.720 1.000 3 2014 2018
dbSNP: rs10088390
rs10088390
SFRP1
2 0.925 0.080 8 41264249 3 prime UTR variant C/G snv 0.19 0.010 1.000 1 2017 2017
dbSNP: rs1011445550
rs1011445550
TP53
2 0.925 0.080 17 7676391 missense variant G/C snv 0.010 1.000 1 2011 2011
dbSNP: rs10116253
rs10116253 		4 0.851 0.120 9 117702042 upstream gene variant T/C snv 0.28 0.010 1.000 1 2014 2014
dbSNP: rs1016343
rs1016343
PCAT1 ; PRNCR1 ; CASC19 ; PCAT2
8 0.807 0.240 8 127081052 non coding transcript exon variant C/T snv 0.20 0.010 1.000 1 2019 2019
dbSNP: rs1042028
rs1042028
SULT1A1
30 0.658 0.440 16 28606193 missense variant C/T snv 0.22 0.30 0.010 1.000 1 2005 2005
dbSNP: rs10421916
rs10421916
INSL3
2 0.925 0.080 19 17818178 intron variant A/G snv 0.69 0.010 1.000 1 2012 2012
dbSNP: rs1042229
rs1042229
FPR1
7 0.790 0.280 19 51746419 missense variant A/C;G snv 0.32; 0.13 0.010 1.000 1 2011 2011
dbSNP: rs1042522
rs1042522
TP53
242 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 0.100 0.900 10 2009 2015
dbSNP: rs10434
rs10434
VEGFA
17 0.701 0.480 6 43785475 3 prime UTR variant A/G snv 0.59 0.010 1.000 1 2009 2009
dbSNP: rs1044432
rs1044432
BTBD10
2 0.925 0.080 11 13388251 3 prime UTR variant A/T snv 0.16 0.010 1.000 1 2019 2019
dbSNP: rs1045411
rs1045411
HMGB1
18 0.708 0.360 13 30459095 3 prime UTR variant C/T snv 0.20 0.010 1.000 1 2016 2016
dbSNP: rs1045642
rs1045642
ABCB1
214 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 0.040 0.750 4 2008 2017
dbSNP: rs10464867
rs10464867
OSGIN2 ; NBN
2 0.925 0.080 8 89933370 3 prime UTR variant C/T snv 3.0E-02 0.010 1.000 1 2015 2015
dbSNP: rs10474606
rs10474606
THBS4
2 0.925 0.080 5 80057163 intron variant G/A snv 0.28 0.010 1.000 1 2016 2016
dbSNP: rs1047768
rs1047768
ERCC5 ; BIVM-ERCC5
20 0.695 0.320 13 102852167 synonymous variant T/C snv 0.52 0.59 0.030 0.667 3 2009 2017
dbSNP: rs1047840
rs1047840
EXO1
19 0.708 0.280 1 241878999 missense variant G/A snv 0.36 0.40 0.010 1.000 1 2009 2009
dbSNP: rs1047972
rs1047972
AURKA
19 0.716 0.240 20 56386407 missense variant T/C snv 0.85 0.84 0.030 1.000 3 2006 2019