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: rs11587591
rs11587591
1.000 0.040 1 209589530 intron variant A/G snv 0.22
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs17014830
rs17014830
1.000 0.040 1 209585282 intron variant T/A snv 0.18
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs7516885
rs7516885
1.000 0.040 1 209591648 intron variant C/T snv 0.17
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs7528476
rs7528476
1.000 0.040 1 209591531 intron variant A/G snv 0.64
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs7528698
rs7528698
1.000 0.040 1 209591742 intron variant A/C;T snv
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs1228276529
rs1228276529
1.000 0.080 1 209612203 missense variant G/A snv
Infiltrating duct carcinoma of female breast
Neoplasms; Skin and Connective Tissue Diseases 0.700 0