Source: ALL

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: rs10203995
rs10203995
ARHGEF33 ; LOC105374471
1.000 0.040 2 38937913 intron variant C/T snv 0.70
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2017 2017
dbSNP: rs368451
rs368451
ARHGEF33 ; LOC105374471
1.000 0.040 2 38939435 intron variant T/C snv 0.93
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2017 2017
dbSNP: rs408686
rs408686
ARHGEF33 ; LOC105374471
1.000 0.040 2 38950179 intron variant C/A;T snv
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2017 2017
dbSNP: rs441869
rs441869
ARHGEF33 ; LOC105374471
1.000 0.040 2 38951352 intron variant G/C snv 0.95
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2017 2017