MLIP, muscular LMNA interacting protein, 90523

N. diseases: 37; N. variants: 19
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: rs9296736
rs9296736 		6 54059899 intron variant T/C snv 0.51
CUI: C1278049
Disease: Serum gamma-glutamyl transferase measurement
Serum gamma-glutamyl transferase measurement 		0.800 1.000 1 2011 2011
dbSNP: rs12191362
rs12191362 		1.000 0.040 6 54047537 non coding transcript exon variant A/G snv 4.0E-02
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs1325831
rs1325831 		1.000 0.040 6 54039549 intron variant T/C snv 0.51
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs1325833
rs1325833 		1.000 0.040 6 54031357 intron variant A/C;G snv
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs1359563
rs1359563 		1.000 0.040 6 54029992 intron variant C/T snv 0.38
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs142295881
rs142295881 		1.000 0.040 6 54034290 intron variant A/G snv 1.1E-02
CUI: C1263846
Disease: Attention deficit hyperactivity disorder
Attention deficit hyperactivity disorder 		Mental Disorders 0.700 1.000 1 2018 2018
dbSNP: rs142516820
rs142516820 		6 54138254 missense variant A/G snv 2.7E-03 9.1E-04
CUI: C0017654
Disease: Glomerular Filtration Rate
Glomerular Filtration Rate 		0.700 1.000 1 2018 2018
dbSNP: rs142516820
rs142516820 		6 54138254 missense variant A/G snv 2.7E-03 9.1E-04
CUI: C0201976
Disease: Creatinine measurement, serum (procedure)
Creatinine measurement, serum (procedure) 		0.700 1.000 1 2018 2018
dbSNP: rs16884633
rs16884633 		1.000 0.040 6 54037373 intron variant G/A snv 0.20
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs7750294
rs7750294 		1.000 0.040 6 54059372 intron variant A/T snv 6.5E-02
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs816366
rs816366 		6 54130706 intron variant C/A;T snv
CUI: C0337443
Disease: Sodium measurement
Sodium measurement 		0.700 1.000 1 2019 2019
dbSNP: rs816367
rs816367 		6 54130744 intron variant G/A;C;T snv
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2019 2019
dbSNP: rs9357785
rs9357785 		1.000 0.040 6 54055973 intron variant A/G;T snv
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs9370259
rs9370259 		1.000 0.040 6 54056608 intron variant T/C snv 0.11
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs9464019
rs9464019 		1.000 0.040 6 54035922 intron variant T/C snv 3.0E-02
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs9637973
rs9637973 		1.000 0.040 6 54038354 intron variant G/A snv 0.51
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs9637973
rs9637973 		1.000 0.040 6 54038354 intron variant G/A snv 0.51
CUI: C1278049
Disease: Serum gamma-glutamyl transferase measurement
Serum gamma-glutamyl transferase measurement 		0.700 1.000 1 2018 2018
dbSNP: rs1770833
rs1770833 		1.000 0.080 6 54167063 intron variant T/C snv
CUI: C0028754
Disease: Obesity
Obesity 		Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases 0.010 < 0.001 1 2008 2008
dbSNP: rs665640
rs665640 		1.000 0.080 6 54122584 intron variant T/A snv 0.39
CUI: C0494463
Disease: Alzheimer Disease, Late Onset
Alzheimer Disease, Late Onset 		Nervous System Diseases; Mental Disorders 0.010 1.000 1 2017 2017
dbSNP: rs770251749
rs770251749 		1.000 0.120 6 54121506 missense variant A/C snv 4.0E-06
CUI: C0027651
Disease: Neoplasms
Neoplasms 		Neoplasms 0.010 1.000 1 1995 1995
dbSNP: rs770251749
rs770251749 		1.000 0.120 6 54121506 missense variant A/C snv 4.0E-06
CUI: C2931822
Disease: Nasopharyngeal carcinoma
Nasopharyngeal carcinoma 		Neoplasms; Stomatognathic Diseases; Otorhinolaryngologic Diseases 0.010 1.000 1 1995 1995
dbSNP: rs9395890
rs9395890 		0.925 0.080 6 53956196 intron variant G/A;T snv
CUI: C0022661
Disease: Kidney Failure, Chronic
Kidney Failure, Chronic 		Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases 0.010 1.000 1 2019 2019
dbSNP: rs9395890
rs9395890 		0.925 0.080 6 53956196 intron variant G/A;T snv
CUI: C2316810
Disease: Chronic kidney disease stage 5
Chronic kidney disease stage 5 		Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases 0.010 1.000 1 2019 2019