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: rs2606345
rs2606345
0.732 0.360 15 74724835 intron variant C/A snv 0.46
CUI: C0032302
Disease: Mycoplasma pneumonia
Mycoplasma pneumonia
0.010 1.000 1 2017 2017
dbSNP: rs2606345
rs2606345
0.732 0.360 15 74724835 intron variant C/A snv 0.46
Respiratory Distress Syndrome, Adult
0.010 1.000 1 2014 2014
dbSNP: rs2606345
rs2606345
0.732 0.360 15 74724835 intron variant C/A snv 0.46
CUI: C0684249
Disease: Carcinoma of lung
Carcinoma of lung
0.010 1.000 1 2009 2009
dbSNP: rs2606345
rs2606345
0.732 0.360 15 74724835 intron variant C/A snv 0.46
CUI: C0949083
Disease: Hospital acquired pneumonia
Hospital acquired pneumonia
0.010 1.000 1 2014 2014
dbSNP: rs2606345
rs2606345
0.732 0.360 15 74724835 intron variant C/A snv 0.46
CUI: C0264490
Disease: Acute respiratory failure
Acute respiratory failure
0.010 1.000 1 2013 2013
dbSNP: rs2606345
rs2606345
0.732 0.360 15 74724835 intron variant C/A snv 0.46
CUI: C0086132
Disease: Depressive Symptoms
Depressive Symptoms
0.010 1.000 1 2006 2006
dbSNP: rs2606345
rs2606345
0.732 0.360 15 74724835 intron variant C/A snv 0.46
CUI: C0242379
Disease: Malignant neoplasm of lung
Malignant neoplasm of lung
0.010 1.000 1 2009 2009
dbSNP: rs2606345
rs2606345
0.732 0.360 15 74724835 intron variant C/A snv 0.46
CUI: C0036572
Disease: Seizures
Seizures
0.010 1.000 1 2010 2010
dbSNP: rs2606345
rs2606345
0.732 0.360 15 74724835 intron variant C/A snv 0.46
CUI: C0740277
Disease: Bile duct carcinoma
Bile duct carcinoma
0.010 1.000 1 2009 2009
dbSNP: rs2606345
rs2606345
0.732 0.360 15 74724835 intron variant C/A snv 0.46
CUI: C0262401
Disease: Carcinoma of ampulla of Vater
Carcinoma of ampulla of Vater
0.010 1.000 1 2009 2009
dbSNP: rs2606345
rs2606345
0.732 0.360 15 74724835 intron variant C/A snv 0.46
CUI: C1335059
Disease: testicular nonseminoma
testicular nonseminoma
0.010 1.000 1 2008 2008
dbSNP: rs2606345
rs2606345
0.732 0.360 15 74724835 intron variant C/A snv 0.46
CUI: C0014544
Disease: Epilepsy
Epilepsy
0.010 1.000 1 2010 2010
dbSNP: rs2606345
rs2606345
0.732 0.360 15 74724835 intron variant C/A snv 0.46
CUI: C1306460
Disease: Primary malignant neoplasm of lung
Primary malignant neoplasm of lung
0.010 1.000 1 2009 2009
dbSNP: rs2606345
rs2606345
0.732 0.360 15 74724835 intron variant C/A snv 0.46
CUI: C0006118
Disease: Brain Neoplasms
Brain Neoplasms
0.010 1.000 1 2013 2013
dbSNP: rs2606345
rs2606345
0.732 0.360 15 74724835 intron variant C/A snv 0.46
CUI: C1855179
Disease: CATARACT, ANTERIOR POLAR
CATARACT, ANTERIOR POLAR
0.010 1.000 1 2013 2013
dbSNP: rs2606345
rs2606345
0.732 0.360 15 74724835 intron variant C/A snv 0.46
CUI: C1443237
Disease: Healthcare associated pneumonia
Healthcare associated pneumonia
0.010 1.000 1 2014 2014