ATF2, activating transcription factor 2, 1386

N. diseases: 122; N. variants: 17
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: rs1153672
rs1153672 		1.000 0.040 2 175122245 intron variant G/A snv 9.3E-02
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs1153676
rs1153676 		1.000 0.040 2 175116266 intron variant C/A;T snv
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs1153681
rs1153681 		1.000 0.040 2 175099859 intron variant G/A snv 9.7E-02
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs1153684
rs1153684 		1.000 0.040 2 175090624 intron variant A/G snv 0.10
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs11888507
rs11888507 		1.000 0.040 2 175147893 intron variant C/T snv 0.27
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs11894840
rs11894840 		1.000 0.040 2 175152337 intron variant G/C snv 9.8E-02
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs13383680
rs13383680 		1.000 0.040 2 175115817 intron variant T/C snv 5.4E-02
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs13388308
rs13388308 		1.000 0.040 2 175141299 intron variant C/T snv 0.26
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs17270532
rs17270532 		1.000 0.040 2 175152468 intron variant A/C;T snv
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs2178329
rs2178329 		1.000 0.040 2 175122951 intron variant G/A snv 0.90
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs2541066
rs2541066 		1.000 0.040 2 175109696 intron variant T/C snv 0.10
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs3771928
rs3771928 		1.000 0.040 2 175120924 intron variant G/A snv 6.7E-02
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs7566401
rs7566401 		1.000 0.040 2 175129992 intron variant C/A snv 0.11
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs7571171
rs7571171 		1.000 0.040 2 175131768 intron variant G/A snv 0.11
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs1231071385
rs1231071385 		1.000 0.040 2 175093177 frameshift variant -/G ins
CUI: C0025202
Disease: melanoma
melanoma 		Neoplasms 0.010 1.000 1 2010 2010
dbSNP: rs3845744
rs3845744 		0.925 0.080 2 175078526 intron variant C/T snv 0.76
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma 		Neoplasms; Skin and Connective Tissue Diseases 0.010 < 0.001 1 2016 2016
dbSNP: rs3845744
rs3845744 		0.925 0.080 2 175078526 intron variant C/T snv 0.76
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast 		Neoplasms; Skin and Connective Tissue Diseases 0.010 < 0.001 1 2016 2016
dbSNP: rs79402775
rs79402775 		0.827 0.200 2 175167648 mature miRNA variant G/A;T snv 4.4E-02; 1.0E-05
CUI: C0154038
Disease: Benign neoplasm of thyroid gland
Benign neoplasm of thyroid gland 		Neoplasms; Endocrine System Diseases 0.010 1.000 1 2015 2015
dbSNP: rs79402775
rs79402775 		0.827 0.200 2 175167648 mature miRNA variant G/A;T snv 4.4E-02; 1.0E-05
CUI: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach 		Digestive System Diseases; Neoplasms 0.010 1.000 1 2019 2019
dbSNP: rs79402775
rs79402775 		0.827 0.200 2 175167648 mature miRNA variant G/A;T snv 4.4E-02; 1.0E-05
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma 		Digestive System Diseases; Neoplasms 0.010 1.000 1 2019 2019
dbSNP: rs79402775
rs79402775 		0.827 0.200 2 175167648 mature miRNA variant G/A;T snv 4.4E-02; 1.0E-05
CUI: C0238463
Disease: Papillary thyroid carcinoma
Papillary thyroid carcinoma 		Neoplasms; Endocrine System Diseases 0.010 1.000 1 2015 2015
dbSNP: rs79402775
rs79402775 		0.827 0.200 2 175167648 mature miRNA variant G/A;T snv 4.4E-02; 1.0E-05
CUI: C0948008
Disease: Ischemic stroke
Ischemic stroke 		Nervous System Diseases; Cardiovascular Diseases 0.010 1.000 1 2019 2019