MXI1, MAX interactor 1, dimerization protein, 4601

N. diseases: 128; N. variants: 11
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: rs137852603
rs137852603 		1.000 0.080 10 110280017 missense variant A/C snv
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate 		Neoplasms; Male Urogenital Diseases 0.800 1.000 5 2008 2015
dbSNP: rs137852604
rs137852604 		0.925 0.080 10 110228276 missense variant C/T snv 4.0E-06 7.0E-06
CUI: C0206729
Disease: Neurofibrosarcoma
Neurofibrosarcoma 		Neoplasms; Nervous System Diseases 0.710 1.000 1 1999 1999
dbSNP: rs111777102
rs111777102 		10 110206068 upstream gene variant C/T snv 5.4E-02
CUI: C0428883
Disease: Diastolic blood pressure
Diastolic blood pressure 		0.700 1.000 1 2018 2018
dbSNP: rs11195062
rs11195062 		10 110277217 intron variant C/A snv 0.41
CUI: C1261502
Disease: Finding of Mean Corpuscular Hemoglobin
Finding of Mean Corpuscular Hemoglobin 		0.700 1.000 1 2019 2019
dbSNP: rs113511609
rs113511609 		10 110210161 intron variant C/A;G;T snv
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure 		0.700 1.000 1 2019 2019
dbSNP: rs1475502
rs1475502 		10 110207797 5 prime UTR variant C/T snv 0.12 6.0E-02
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs17127170
rs17127170 		10 110232464 intron variant T/A;C snv
CUI: C0032181
Disease: Platelet Count measurement
Platelet Count measurement 		0.700 1.000 1 2018 2018
dbSNP: rs1967840
rs1967840 		10 110266324 intron variant A/G snv 0.21
CUI: C0005612
Disease: Birth Weight
Birth Weight 		Pathological Conditions, Signs and Symptoms 0.700 1.000 1 2019 2019
dbSNP: rs2855469
rs2855469 		10 110281821 intron variant T/C snv 0.43
CUI: C0007222
Disease: Cardiovascular Diseases
Cardiovascular Diseases 		Cardiovascular Diseases 0.700 1.000 1 2019 2019
dbSNP: rs387906417
rs387906417 		1.000 0.080 10 110279296 splice donor variant T/C snv
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate 		Neoplasms; Male Urogenital Diseases 0.700 0
dbSNP: rs137852604
rs137852604 		0.925 0.080 10 110228276 missense variant C/T snv 4.0E-06 7.0E-06
CUI: C0751690
Disease: Malignant Peripheral Nerve Sheath Tumor
Malignant Peripheral Nerve Sheath Tumor 		Neoplasms; Nervous System Diseases 0.010 1.000 1 1999 1999
dbSNP: rs759049323
rs759049323 		0.925 0.080 10 110284872 missense variant T/C;G snv 4.0E-06; 4.0E-06
CUI: C0206729
Disease: Neurofibrosarcoma
Neurofibrosarcoma 		Neoplasms; Nervous System Diseases 0.010 1.000 1 1999 1999
dbSNP: rs759049323
rs759049323 		0.925 0.080 10 110284872 missense variant T/C;G snv 4.0E-06; 4.0E-06
CUI: C0751690
Disease: Malignant Peripheral Nerve Sheath Tumor
Malignant Peripheral Nerve Sheath Tumor 		Neoplasms; Nervous System Diseases 0.010 1.000 1 1999 1999