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: rs10501383
rs10501383
MS4A14
1.000 0.040 11 60397054 intron variant C/T snv 5.7E-02
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2017 2017
dbSNP: rs10897056
rs10897056
MS4A14
1.000 0.040 11 60398982 intron variant A/G snv 0.71
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2017 2017
dbSNP: rs2233244
rs2233244
MS4A7 ; MS4A14
1.000 0.040 11 60385058 intron variant A/C;T snv 0.23; 1.2E-05
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2017 2017
dbSNP: rs2241920
rs2241920
MS4A14
1.000 0.040 11 60396731 intron variant G/A snv 0.65 0.62
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2017 2017
dbSNP: rs3816270
rs3816270
MS4A7 ; MS4A14
1.000 0.040 11 60396162 5 prime UTR variant T/C snv 0.76
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2017 2017
dbSNP: rs4939352
rs4939352
MS4A14
1.000 0.040 11 60405634 intron variant A/G snv 0.67
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2017 2017
dbSNP: rs7107802
rs7107802
MS4A14
1.000 0.040 11 60399149 intron variant T/C snv 0.69
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2017 2017
dbSNP: rs950802
rs950802
MS4A7 ; MS4A14
1.000 0.040 11 60385111 synonymous variant G/A snv 0.35 0.36
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2017 2017
dbSNP: rs950803
rs950803
MS4A7 ; MS4A14
1.000 0.040 11 60385090 splice region variant T/A snv 0.64 0.60
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2017 2017
dbSNP: rs7935082
rs7935082
MS4A7 ; MS4A14
1.000 0.040 11 60387527 intron variant T/C snv 0.62
CUI: C0011847
Disease: Diabetes
Diabetes 		0.010 1.000 1 2007 2007
dbSNP: rs7935082
rs7935082
MS4A7 ; MS4A14
1.000 0.040 11 60387527 intron variant T/C snv 0.62
CUI: C0011849
Disease: Diabetes Mellitus
Diabetes Mellitus 		0.010 1.000 1 2007 2007