Source: BEFREE

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: rs344781
rs344781
0.807 0.200 19 43670636 upstream gene variant C/T snv 0.80
CUI: C0338480
Disease: Common Migraine
Common Migraine
0.010 1.000 1 2014 2014
dbSNP: rs344781
rs344781
0.807 0.200 19 43670636 upstream gene variant C/T snv 0.80
CUI: C0018681
Disease: Headache
Headache
0.010 1.000 1 2014 2014
dbSNP: rs344781
rs344781
0.807 0.200 19 43670636 upstream gene variant C/T snv 0.80
CUI: C0007131
Disease: Non-Small Cell Lung Carcinoma
Non-Small Cell Lung Carcinoma
0.010 1.000 1 2011 2011
dbSNP: rs344781
rs344781
0.807 0.200 19 43670636 upstream gene variant C/T snv 0.80
Idiopathic pulmonary arterial hypertension
0.010 1.000 1 2011 2011
dbSNP: rs344781
rs344781
0.807 0.200 19 43670636 upstream gene variant C/T snv 0.80
CUI: C1510586
Disease: Autism Spectrum Disorders
Autism Spectrum Disorders
0.010 1.000 1 2008 2008
dbSNP: rs344781
rs344781
0.807 0.200 19 43670636 upstream gene variant C/T snv 0.80
CUI: C0036421
Disease: Systemic Scleroderma
Systemic Scleroderma
0.010 1.000 1 2011 2011
dbSNP: rs344781
rs344781
0.807 0.200 19 43670636 upstream gene variant C/T snv 0.80
CUI: C0007137
Disease: Squamous cell carcinoma
Squamous cell carcinoma
0.010 1.000 1 2016 2016