Source: BEFREE

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs17655
rs17655
0.597 0.560 13 102875652 missense variant G/C snv 0.28 0.30
CUI: C0024299
Disease: Lymphoma
Lymphoma
0.010 < 0.001 1 2013 2013
dbSNP: rs1042522
rs1042522
0.426 0.800 17 7676154 missense variant G/C;T snv 0.67
CUI: C0024299
Disease: Lymphoma
Lymphoma
0.010 1.000 1 2012 2012
dbSNP: rs2395185
rs2395185
0.724 0.360 6 32465390 intron variant G/T snv 0.29
CUI: C0024299
Disease: Lymphoma
Lymphoma
0.010 1.000 1 2015 2015
dbSNP: rs2466571
rs2466571
0.925 0.120 1 207766701 intron variant G/T snv 0.46
CUI: C0024299
Disease: Lymphoma
Lymphoma
0.010 1.000 1 2014 2014
dbSNP: rs878854066
rs878854066
0.439 0.800 17 7676153 missense variant GG/AC mnv
CUI: C0024299
Disease: Lymphoma
Lymphoma
0.010 1.000 1 2012 2012
dbSNP: rs6676671
rs6676671
0.882 0.160 1 206779403 intron variant T/A snv 0.32
CUI: C0024299
Disease: Lymphoma
Lymphoma
0.010 1.000 1 2008 2008
dbSNP: rs1802710
rs1802710
14 100734308 synonymous variant T/A;C snv 0.63
CUI: C0024299
Disease: Lymphoma
Lymphoma
0.010 1.000 1 2004 2004
dbSNP: rs267601394
rs267601394
0.807 0.200 7 148811635 missense variant T/A;G snv
CUI: C0024299
Disease: Lymphoma
Lymphoma
0.720 1.000 2 2012 2016
dbSNP: rs13181
rs13181
0.487 0.760 19 45351661 stop gained T/A;G snv 4.0E-06; 0.32
CUI: C0024299
Disease: Lymphoma
Lymphoma
0.010 1.000 1 2009 2009
dbSNP: rs387907272
rs387907272
0.572 0.520 3 38141150 stop lost T/C snv 5.2E-05 7.0E-06
CUI: C0024299
Disease: Lymphoma
Lymphoma
0.100 0.917 12 2013 2019
dbSNP: rs1800896
rs1800896
0.507 0.800 1 206773552 intron variant T/C snv 0.41
CUI: C0024299
Disease: Lymphoma
Lymphoma
0.020 1.000 2 2008 2010
dbSNP: rs25487
rs25487
0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71
CUI: C0024299
Disease: Lymphoma
Lymphoma
0.020 1.000 2 2004 2011
dbSNP: rs662
rs662
0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42
CUI: C0024299
Disease: Lymphoma
Lymphoma
0.020 1.000 2 2013 2015
dbSNP: rs1346044
rs1346044
WRN
0.708 0.440 8 31167138 missense variant T/C snv 0.24 0.23
CUI: C0024299
Disease: Lymphoma
Lymphoma
0.010 1.000 1 2006 2006
dbSNP: rs1555525126
rs1555525126
0.925 0.120 17 7673749 missense variant T/C snv
CUI: C0024299
Disease: Lymphoma
Lymphoma
0.010 1.000 1 2001 2001
dbSNP: rs1883832
rs1883832
0.581 0.680 20 46118343 5 prime UTR variant T/C snv 0.75 0.80
CUI: C0024299
Disease: Lymphoma
Lymphoma
0.010 1.000 1 2008 2008
dbSNP: rs707824
rs707824
0.925 0.120 6 14636732 intergenic variant T/C snv 0.74
CUI: C0024299
Disease: Lymphoma
Lymphoma
0.810 1.000 1 2013 2013
dbSNP: rs751837
rs751837
0.882 0.120 14 103018488 intron variant T/C snv 0.23
CUI: C0024299
Disease: Lymphoma
Lymphoma
0.010 1.000 1 2011 2011
dbSNP: rs867114783
rs867114783
17 7675109 missense variant T/C snv
CUI: C0024299
Disease: Lymphoma
Lymphoma
0.010 1.000 1 2014 2014
dbSNP: rs2230926
rs2230926
0.662 0.440 6 137874929 missense variant T/C;G snv 4.0E-06; 5.4E-02
CUI: C0024299
Disease: Lymphoma
Lymphoma
0.040 1.000 4 2013 2019
dbSNP: rs1800975
rs1800975
XPA
0.701 0.360 9 97697296 5 prime UTR variant T/C;G snv 0.63; 4.5E-06; 4.5E-06
CUI: C0024299
Disease: Lymphoma
Lymphoma
0.010 < 0.001 1 2013 2013
dbSNP: rs61754966
rs61754966
NBN
0.701 0.280 8 89978293 missense variant T/C;G snv 1.2E-03
CUI: C0024299
Disease: Lymphoma
Lymphoma
0.010 1.000 1 2008 2008
dbSNP: rs397507444
rs397507444
0.405 0.880 1 11794407 missense variant T/G snv
CUI: C0024299
Disease: Lymphoma
Lymphoma
0.050 1.000 5 2004 2017
dbSNP: rs1800872
rs1800872
0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69
CUI: C0024299
Disease: Lymphoma
Lymphoma
0.020 1.000 2 2008 2010
dbSNP: rs1946518
rs1946518
0.602 0.760 11 112164735 intron variant T/G snv 0.60
CUI: C0024299
Disease: Lymphoma
Lymphoma
0.010 1.000 1 2017 2017