Source: UNIPROT

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: rs104894421
rs104894421
LIG4
0.882 0.200 13 108210436 missense variant C/A;T snv 1.2E-05
CUI: C0023418
Disease: leukemia
leukemia 		0.700 0
dbSNP: rs121913250
rs121913250
NRAS
0.683 0.440 1 114716127 missense variant C/A;G;T snv
CUI: C0023418
Disease: leukemia
leukemia 		0.700 0
dbSNP: rs61753793
rs61753793
MSH6 ; FBXO11
0.851 0.120 2 47799002 missense variant T/C snv 3.6E-05 5.6E-05
CUI: C0023418
Disease: leukemia
leukemia 		0.700 0
dbSNP: rs6413463
rs6413463
CDKN2A
1.000 0.040 9 21970990 missense variant A/G;T snv 2.9E-05; 3.0E-04
CUI: C0023418
Disease: leukemia
leukemia 		0.700 0