Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs2227306
rs2227306
0.677 0.680 4 73741338 intron variant C/T snv 0.31
CUI: C0018213
Disease: Graves Disease
Graves Disease
0.010 1.000 1 2009 2009
dbSNP: rs2227306
rs2227306
0.677 0.680 4 73741338 intron variant C/T snv 0.31
CUI: C0339143
Disease: Thyroid associated opthalmopathies
Thyroid associated opthalmopathies
0.010 1.000 1 2009 2009
dbSNP: rs4073
rs4073
0.566 0.800 4 73740307 upstream gene variant A/T snv 0.46
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate
0.050 0.800 5 2010 2019
dbSNP: rs4073
rs4073
0.566 0.800 4 73740307 upstream gene variant A/T snv 0.46
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma
0.050 0.800 5 2010 2019
dbSNP: rs2227306
rs2227306
0.677 0.680 4 73741338 intron variant C/T snv 0.31
CUI: C0206139
Disease: Lichen Planus, Oral
Lichen Planus, Oral
0.010 1.000 1 2010 2010
dbSNP: rs2227306
rs2227306
0.677 0.680 4 73741338 intron variant C/T snv 0.31
CUI: C0017661
Disease: IGA Glomerulonephritis
IGA Glomerulonephritis
0.010 1.000 1 2011 2011
dbSNP: rs2227306
rs2227306
0.677 0.680 4 73741338 intron variant C/T snv 0.31
CUI: C1800706
Disease: Idiopathic Pulmonary Fibrosis
Idiopathic Pulmonary Fibrosis
0.010 1.000 1 2011 2011
dbSNP: rs2227307
rs2227307
0.851 0.240 4 73740952 intron variant T/G snv 0.45
CUI: C1800706
Disease: Idiopathic Pulmonary Fibrosis
Idiopathic Pulmonary Fibrosis
0.010 1.000 1 2011 2011
dbSNP: rs2227543
rs2227543
1.000 0.120 4 73742193 3 prime UTR variant C/T snv 0.32
CUI: C0017661
Disease: IGA Glomerulonephritis
IGA Glomerulonephritis
0.010 1.000 1 2011 2011
dbSNP: rs4073
rs4073
0.566 0.800 4 73740307 upstream gene variant A/T snv 0.46
CUI: C0042580
Disease: Vesico-Ureteral Reflux
Vesico-Ureteral Reflux
0.010 1.000 1 2011 2011
dbSNP: rs4073
rs4073
0.566 0.800 4 73740307 upstream gene variant A/T snv 0.46
CUI: C0266929
Disease: Chronic Periodontitis
Chronic Periodontitis
0.010 1.000 1 2011 2011
dbSNP: rs4073
rs4073
0.566 0.800 4 73740307 upstream gene variant A/T snv 0.46
CUI: C0011206
Disease: Delirium
Delirium
0.010 < 0.001 1 2011 2011
dbSNP: rs4073
rs4073
0.566 0.800 4 73740307 upstream gene variant A/T snv 0.46
CUI: C0039494
Disease: Temporomandibular Joint Disorders
Temporomandibular Joint Disorders
0.010 1.000 1 2011 2011
dbSNP: rs4073
rs4073
0.566 0.800 4 73740307 upstream gene variant A/T snv 0.46
CUI: C0520575
Disease: Acute pyelonephritis
Acute pyelonephritis
0.010 1.000 1 2011 2011
dbSNP: rs4073
rs4073
0.566 0.800 4 73740307 upstream gene variant A/T snv 0.46
CUI: C3266959
Disease: Acute focal bacterial nephritis
Acute focal bacterial nephritis
0.010 1.000 1 2011 2011
dbSNP: rs4073
rs4073
0.566 0.800 4 73740307 upstream gene variant A/T snv 0.46
CUI: C1800706
Disease: Idiopathic Pulmonary Fibrosis
Idiopathic Pulmonary Fibrosis
0.010 1.000 1 2011 2011
dbSNP: rs4073
rs4073
0.566 0.800 4 73740307 upstream gene variant A/T snv 0.46
CUI: C0017661
Disease: IGA Glomerulonephritis
IGA Glomerulonephritis
0.010 1.000 1 2011 2011
dbSNP: rs4073
rs4073
0.566 0.800 4 73740307 upstream gene variant A/T snv 0.46
CUI: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach
0.040 1.000 4 2012 2018
dbSNP: rs4073
rs4073
0.566 0.800 4 73740307 upstream gene variant A/T snv 0.46
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
0.040 1.000 4 2012 2018
dbSNP: rs2227544
rs2227544
4 73742906 3 prime UTR variant G/A snv 4.4E-03
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.700 1.000 1 2012 2012
dbSNP: rs4073
rs4073
0.566 0.800 4 73740307 upstream gene variant A/T snv 0.46
CUI: C0001339
Disease: Acute pancreatitis
Acute pancreatitis
0.020 1.000 2 2013 2019
dbSNP: rs4073
rs4073
0.566 0.800 4 73740307 upstream gene variant A/T snv 0.46
CUI: C0031106
Disease: Aggressive Periodontitis
Aggressive Periodontitis
0.010 < 0.001 1 2013 2013
dbSNP: rs4073
rs4073
0.566 0.800 4 73740307 upstream gene variant A/T snv 0.46
CUI: C0001342
Disease: Acute periodontitis
Acute periodontitis
0.010 < 0.001 1 2013 2013
dbSNP: rs4073
rs4073
0.566 0.800 4 73740307 upstream gene variant A/T snv 0.46
Aggressive periodontitis, generalized
0.010 1.000 1 2013 2013
dbSNP: rs780209935
rs780209935
1.000 0.040 4 73742000 stop gained G/A snv 8.0E-06
CUI: C0679408
Disease: Lesion of stomach
Lesion of stomach
0.010 < 0.001 1 2013 2013