Disease: Neoplasms ×
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs113488022
rs113488022 		0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06
CUI: C0027651
Disease: Neoplasms
Neoplasms 		Neoplasms 0.800 0.947 475 2003 2020
dbSNP: rs121913364
rs121913364 		0.641 0.520 7 140753334 missense variant T/C;G snv 4.0E-06
CUI: C0027651
Disease: Neoplasms
Neoplasms 		Neoplasms 0.780 0.778 9 2004 2019
dbSNP: rs121913355
rs121913355 		0.641 0.520 7 140781602 missense variant C/A;G;T snv 4.0E-06
CUI: C0027651
Disease: Neoplasms
Neoplasms 		Neoplasms 0.730 0.800 5 2004 2015
dbSNP: rs121913348
rs121913348 		0.763 0.480 7 140781617 missense variant C/A;G;T snv
CUI: C0027651
Disease: Neoplasms
Neoplasms 		Neoplasms 0.720 1.000 3 2004 2016
dbSNP: rs121913335
rs121913335 		7 140753375 missense variant T/G snv
CUI: C0027651
Disease: Neoplasms
Neoplasms 		Neoplasms 0.700 1.000 1 2014 2014
dbSNP: rs121913336
rs121913336 		7 140753374 missense variant G/C;T snv
CUI: C0027651
Disease: Neoplasms
Neoplasms 		Neoplasms 0.700 1.000 1 2014 2014
dbSNP: rs121913341
rs121913341 		0.851 0.280 7 140753350 missense variant A/C;T snv
CUI: C0027651
Disease: Neoplasms
Neoplasms 		Neoplasms 0.700 1.000 1 2004 2004
dbSNP: rs121913362
rs121913362 		7 140753359 missense variant T/C snv
CUI: C0027651
Disease: Neoplasms
Neoplasms 		Neoplasms 0.700 1.000 1 2014 2014
dbSNP: rs121913369
rs121913369 		0.790 0.280 7 140753346 missense variant G/A;C snv 4.0E-06
CUI: C0027651
Disease: Neoplasms
Neoplasms 		Neoplasms 0.700 1.000 1 2004 2004
dbSNP: rs121913375
rs121913375 		0.851 0.240 7 140753339 missense variant G/A;C snv
CUI: C0027651
Disease: Neoplasms
Neoplasms 		Neoplasms 0.700 1.000 1 2004 2004
dbSNP: rs121913377
rs121913377 		0.354 0.840 7 140753335 missense variant CA/AT;TT mnv
CUI: C0027651
Disease: Neoplasms
Neoplasms 		Neoplasms 0.100 0.946 465 2003 2020
dbSNP: rs121913227
rs121913227 		0.653 0.320 7 140753336 missense variant AC/CT;TT mnv
CUI: C0027651
Disease: Neoplasms
Neoplasms 		Neoplasms 0.060 1.000 6 2013 2017
dbSNP: rs121913378
rs121913378 		0.776 0.280 7 140753337 missense variant C/A;G;T snv
CUI: C0027651
Disease: Neoplasms
Neoplasms 		Neoplasms 0.020 1.000 2 2007 2012
dbSNP: rs1225976306
rs1225976306 		0.807 0.160 7 140924673 missense variant C/T snv 9.3E-06
CUI: C0027651
Disease: Neoplasms
Neoplasms 		Neoplasms 0.020 1.000 2 2011 2016
dbSNP: rs1057519719
rs1057519719 		1.000 0.080 7 140781593 missense variant T/C snv
CUI: C0027651
Disease: Neoplasms
Neoplasms 		Neoplasms 0.010 1.000 1 2012 2012
dbSNP: rs114729114
rs114729114 		0.925 0.080 7 140910797 intron variant C/T snv 1.1E-02
CUI: C0027651
Disease: Neoplasms
Neoplasms 		Neoplasms 0.010 1.000 1 2016 2016
dbSNP: rs121913338
rs121913338 		0.677 0.400 7 140753354 missense variant T/A;C;G snv
CUI: C0027651
Disease: Neoplasms
Neoplasms 		Neoplasms 0.010 1.000 1 2009 2009
dbSNP: rs121913353
rs121913353 		0.925 0.160 7 140781612 missense variant C/G;T snv
CUI: C0027651
Disease: Neoplasms
Neoplasms 		Neoplasms 0.010 < 0.001 1 2014 2014
dbSNP: rs121913366
rs121913366 		0.763 0.400 7 140753345 missense variant A/C;T snv
CUI: C0027651
Disease: Neoplasms
Neoplasms 		Neoplasms 0.010 1.000 1 2002 2002
dbSNP: rs397507477
rs397507477 		1.000 0.160 7 140777995 missense variant G/A snv
CUI: C0027651
Disease: Neoplasms
Neoplasms 		Neoplasms 0.010 1.000 1 2011 2011