IQCM, IQ motif containing M, 285423

N. diseases: 6; N. variants: 12
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: rs10030601
rs10030601 		1.000 0.040 4 149804060 intron variant T/C snv 0.22
CUI: C0014544
Disease: Epilepsy
Epilepsy 		Nervous System Diseases 0.800 1.000 1 2012 2012
dbSNP: rs10003632
rs10003632 		4 149563756 missense variant G/T snv 4.1E-02
CUI: C0428886
Disease: Mean blood pressure
Mean blood pressure 		0.700 1.000 1 2012 2012
dbSNP: rs1032823
rs1032823 		1.000 0.040 4 149511170 intron variant C/T snv 0.15
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs1503713
rs1503713 		1.000 0.040 4 149446985 intron variant T/C snv 0.15
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs1553427
rs1553427 		1.000 0.040 4 149511763 intron variant T/C snv 0.81
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs17026425
rs17026425 		0.882 0.080 4 149751362 intron variant G/A snv 4.9E-02
CUI: C0034885
Disease: Rectal Neoplasms
Rectal Neoplasms 		Digestive System Diseases; Neoplasms 0.700 1.000 1 2015 2015
dbSNP: rs17026425
rs17026425 		0.882 0.080 4 149751362 intron variant G/A snv 4.9E-02
CUI: C0007113
Disease: Rectal Carcinoma
Rectal Carcinoma 		Digestive System Diseases; Neoplasms 0.700 1.000 1 2015 2015
dbSNP: rs17488863
rs17488863 		1.000 0.040 4 149436564 intron variant T/A snv 0.39
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs17624758
rs17624758 		1.000 0.040 4 149465040 intron variant T/C snv 0.15
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs17686774
rs17686774 		1.000 0.040 4 149499310 intron variant C/A snv 0.14
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs1910462
rs1910462 		1.000 0.040 4 149509171 intron variant G/A snv 0.97
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs4835580
rs4835580 		1.000 0.080 4 149426421 intron variant C/T snv 0.47
CUI: C0027404
Disease: Narcolepsy
Narcolepsy 		Nervous System Diseases; Mental Disorders 0.700 1.000 1 2009 2009
dbSNP: rs4835587
rs4835587 		1.000 0.040 4 149518863 intron variant A/G snv 0.53
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs17026425
rs17026425 		0.882 0.080 4 149751362 intron variant G/A snv 4.9E-02
CUI: C4722085
Disease: Malignant neoplasm of colon and/or rectum
Malignant neoplasm of colon and/or rectum 		0.010 1.000 1 2019 2019
dbSNP: rs17026425
rs17026425 		0.882 0.080 4 149751362 intron variant G/A snv 4.9E-02
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		Digestive System Diseases; Neoplasms 0.010 1.000 1 2019 2019