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: rs10069690
rs10069690
TERT
53 0.595 0.560 5 1279675 intron variant C/T snv 0.36 0.010 1.000 1 2016 2016
dbSNP: rs10822013
rs10822013
ZNF365
4 0.851 0.080 10 62492218 intron variant C/T snv 0.42 0.010 1.000 1 2016 2016
dbSNP: rs11251942
rs11251942
LOC105376360
1 1.000 10 3554755 intron variant G/A snv 0.36 0.700 1.000 1 2019 2019
dbSNP: rs12443621
rs12443621
TOX3
6 0.807 0.120 16 52514125 intron variant A/G snv 0.48 0.010 1.000 1 2010 2010
dbSNP: rs12938141
rs12938141
RAP1GAP2
1 1.000 17 3000998 intron variant T/A;G snv 0.700 1.000 1 2019 2019
dbSNP: rs13267382
rs13267382
LINC00536
3 0.882 0.080 8 116197325 intron variant A/G snv 0.45 0.010 1.000 1 2017 2017
dbSNP: rs140538758
rs140538758
CBFB
1 1.000 16 67082698 intron variant C/G snv 1.5E-02 0.700 1.000 1 2019 2019
dbSNP: rs142697907
rs142697907
PTPN14
1 1.000 1 214510163 intron variant A/G snv 1.0E-02 0.010 1.000 1 2016 2016
dbSNP: rs1432679
rs1432679
EBF1
4 0.851 0.080 5 158817075 intron variant C/T snv 0.44 0.010 1.000 1 2016 2016
dbSNP: rs16917302
rs16917302
ZNF365
5 0.851 0.080 10 62501439 intron variant A/C snv 0.18 0.010 1.000 1 2012 2012
dbSNP: rs2051579
rs2051579
RBFOX2
1 1.000 22 35835310 intron variant G/A;T snv 0.010 1.000 1 2013 2013
dbSNP: rs2268578
rs2268578
LUM
3 0.882 0.080 12 91107421 intron variant A/G snv 0.71 0.010 1.000 1 2008 2008
dbSNP: rs2456773
rs2456773
CDK1
1 1.000 10 60787260 intron variant C/G snv 0.30 0.010 1.000 1 2016 2016
dbSNP: rs250108
rs250108
FGF1 ; SPRY4-AS1
2 0.925 5 142614908 intron variant G/A snv 0.24 0.010 1.000 1 2013 2013
dbSNP: rs2981579
rs2981579
FGFR2
8 0.776 0.280 10 121577821 intron variant A/G snv 0.53 0.700 1.000 1 2017 2017
dbSNP: rs2981582
rs2981582
FGFR2
21 0.695 0.360 10 121592803 intron variant A/G snv 0.58 0.010 1.000 1 2013 2013
dbSNP: rs4783673
rs4783673
CDH1
1 1.000 16 68758190 intron variant T/C;G snv 0.010 1.000 1 2016 2016
dbSNP: rs587150
rs587150 		1 1.000 6 167818409 intron variant G/A snv 0.89 0.700 1.000 1 2019 2019
dbSNP: rs62235635
rs62235635
PITPNB ; TTC28-AS1 ; MIR3199-2
2 0.925 0.080 22 27918624 intron variant G/A snv 4.9E-03 0.700 1.000 1 2019 2019
dbSNP: rs6788895
rs6788895
SIAH2
3 0.882 0.080 3 150750021 intron variant G/T snv 0.18 0.010 1.000 1 2013 2013
dbSNP: rs6828523
rs6828523
ADAM29
4 0.851 0.080 4 174925275 intron variant C/A snv 0.20 0.010 1.000 1 2014 2014
dbSNP: rs6905370
rs6905370
ESR1
2 0.925 6 152005062 intron variant G/A snv 0.38 0.010 1.000 1 2008 2008
dbSNP: rs704010
rs704010
ZMIZ1
4 0.851 0.080 10 79081391 intron variant T/C snv 0.71 0.010 1.000 1 2016 2016
dbSNP: rs7082321
rs7082321
SFMBT2
1 1.000 10 7272478 intron variant C/T snv 0.60 0.700 1.000 1 2019 2019
dbSNP: rs73370840
rs73370840
SLC19A1 ; COL18A1
1 1.000 21 45497121 intron variant C/T snv 0.14 0.16 0.700 1.000 1 2019 2019