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: rs10060683
rs10060683 		1 1.000 0.160 5 92523322 intron variant T/C snv 0.19 0.700 1.000 1 2012 2012
dbSNP: rs1027643
rs1027643
LOC105379082
1 1.000 0.160 5 92558085 intron variant C/T snv 0.19 0.800 1.000 1 2012 2012
dbSNP: rs10767935
rs10767935
WT1
1 1.000 0.160 11 32405158 intron variant C/T snv 0.27 0.010 1.000 1 2015 2015
dbSNP: rs110419
rs110419
LMO1 ; LOC105376536
8 0.827 0.200 11 8231306 intron variant A/G snv 0.42 0.010 1.000 1 2017 2017
dbSNP: rs11913239
rs11913239
TCN2
1 1.000 0.160 22 30613852 intron variant C/T snv 0.12 0.700 1.000 1 2012 2012
dbSNP: rs16988855
rs16988855
TCN2
1 1.000 0.160 22 30615936 intron variant T/C snv 0.12 0.700 1.000 1 2012 2012
dbSNP: rs1799937
rs1799937
WT1
3 0.882 0.160 11 32389228 intron variant A/G snv 0.35 0.35 0.010 1.000 1 2005 2005
dbSNP: rs2009857
rs2009857
TCN2
1 1.000 0.160 22 30618390 intron variant C/G;T snv 0.700 1.000 1 2012 2012
dbSNP: rs2168101
rs2168101
LMO1 ; LOC105376536
7 0.827 0.200 11 8233861 intron variant C/A snv 0.24 0.010 1.000 1 2019 2019
dbSNP: rs2221269
rs2221269
LOC105379082
1 1.000 0.160 5 92571299 intron variant A/G snv 7.3E-02 0.700 1.000 1 2012 2012
dbSNP: rs2267166
rs2267166
TCN2
1 1.000 0.160 22 30622091 intron variant G/A snv 0.11 0.700 1.000 1 2012 2012
dbSNP: rs2283873
rs2283873
TCN2
1 1.000 0.160 22 30617309 intron variant G/A snv 8.8E-02 0.12 0.800 1.000 1 2012 2012
dbSNP: rs2301254
rs2301254
WT1 ; WT1-AS
3 0.882 0.160 11 32436129 intron variant A/G snv 0.48 0.010 1.000 1 2005 2005
dbSNP: rs2857461
rs2857461
EWSR1
3 0.882 0.160 22 29272015 intron variant C/T snv 0.98 0.010 1.000 1 2012 2012
dbSNP: rs28647582
rs28647582
PHOX2B ; PHOX2B-AS1
3 0.882 0.200 4 41747248 intron variant T/C snv 0.38 0.010 1.000 1 2019 2019
dbSNP: rs314276
rs314276
LIN28B
10 0.807 0.280 6 104960124 intron variant A/C snv 0.65 0.010 1.000 1 2018 2018
dbSNP: rs5030244
rs5030244
WT1
1 1.000 0.160 11 32402206 intron variant T/C snv 4.6E-02 0.010 1.000 1 2015 2015
dbSNP: rs57961569
rs57961569
MYCN ; MYCNOS
5 0.827 0.200 2 15939643 intron variant G/A;C snv 0.010 1.000 1 2019 2019
dbSNP: rs5955543
rs5955543
NHS
1 1.000 0.160 X 17680277 intron variant A/G snv 0.17 0.800 1.000 1 2012 2012
dbSNP: rs61344503
rs61344503
LOC105379082
1 1.000 0.160 5 92568740 intron variant G/T snv 0.19 0.700 1.000 1 2012 2012
dbSNP: rs6581658
rs6581658
HMGA2 ; RPSAP52
2 0.925 0.160 12 65823565 intron variant A/G snv 0.14 0.010 1.000 1 2019 2019
dbSNP: rs6887553
rs6887553 		1 1.000 0.160 5 92510102 intron variant A/G snv 0.19 0.700 1.000 1 2012 2012
dbSNP: rs7288385
rs7288385
TCN2
1 1.000 0.160 22 30619586 intron variant C/A snv 0.11 0.700 1.000 1 2012 2012
dbSNP: rs7288627
rs7288627
TCN2
1 1.000 0.160 22 30619575 intron variant G/A snv 0.11 0.700 1.000 1 2012 2012
dbSNP: rs790356
rs790356
DLG2
1 1.000 0.160 11 83909744 intron variant A/G snv 0.50 0.800 1.000 1 2012 2012