rs4988235, MCM6

N. diseases: 19
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
LACTASE PERSISTENCE
CUI: C1857231
Disease: LACTASE PERSISTENCE
9 0.752 0.400 2 135851076 intron variant G/A;C snv 0.800 0.941 17 2009 2019
Blood Protein Measurement
CUI: C2985280
Disease: Blood Protein Measurement
2575 0.752 0.400 2 135851076 intron variant G/A;C snv 0.700 1.000 2 2018 2018
Body mass index
CUI: C1305855
Disease: Body mass index
2689 0.752 0.400 2 135851076 intron variant G/A;C snv 0.700 1.000 2 2015 2018
Hip circumference
CUI: C0562350
Disease: Hip circumference
116 0.752 0.400 2 135851076 intron variant G/A;C snv 0.700 1.000 1 2015 2015
Obesity
CUI: C0028754
Disease: Obesity
1111 0.752 0.400 2 135851076 intron variant G/A;C snv 0.040 1.000 4 2011 2017
Congenital Abnormality
CUI: C0000768
Disease: Congenital Abnormality
73 0.752 0.400 2 135851076 intron variant G/A;C snv 0.010 1.000 1 2019 2019
Congenital defects
CUI: C0220810
Disease: Congenital defects
6 0.752 0.400 2 135851076 intron variant G/A;C snv 0.010 1.000 1 2019 2019
Conventional (Clear Cell) Renal Cell Carcinoma
222 0.752 0.400 2 135851076 intron variant G/A;C snv 0.010 1 2010 2010
Diabetes Mellitus, Non-Insulin-Dependent
2672 0.752 0.400 2 135851076 intron variant G/A;C snv 0.010 1.000 1 2017 2017
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
1085 0.752 0.400 2 135851076 intron variant G/A;C snv 0.010 1 2017 2017
Irritable Bowel Syndrome
CUI: C0022104
Disease: Irritable Bowel Syndrome
52 0.752 0.400 2 135851076 intron variant G/A;C snv 0.010 1.000 1 2009 2009
Malignant neoplasm of prostate
CUI: C0376358
Disease: Malignant neoplasm of prostate
1082 0.752 0.400 2 135851076 intron variant G/A;C snv 0.010 1.000 1 2013 2013
Metabolic Diseases
CUI: C0025517
Disease: Metabolic Diseases
50 0.752 0.400 2 135851076 intron variant G/A;C snv 0.010 1.000 1 2013 2013
Myocardial Ischemia
CUI: C0151744
Disease: Myocardial Ischemia
103 0.752 0.400 2 135851076 intron variant G/A;C snv 0.010 1.000 1 2017 2017
Neural Tube Defects
CUI: C0027794
Disease: Neural Tube Defects
122 0.752 0.400 2 135851076 intron variant G/A;C snv 0.010 1.000 1 2019 2019
Osteoporosis
CUI: C0029456
Disease: Osteoporosis
182 0.752 0.400 2 135851076 intron variant G/A;C snv 0.010 1.000 1 2017 2017
Primary lactose intolerance
CUI: C0342759
Disease: Primary lactose intolerance
1 0.752 0.400 2 135851076 intron variant G/A;C snv 0.010 1.000 1 2013 2013
Prostate carcinoma
CUI: C0600139
Disease: Prostate carcinoma
1168 0.752 0.400 2 135851076 intron variant G/A;C snv 0.010 1.000 1 2013 2013
Renal Cell Carcinoma
CUI: C0007134
Disease: Renal Cell Carcinoma
288 0.752 0.400 2 135851076 intron variant G/A;C snv 0.010 1 2010 2010