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: rs4541843
rs4541843
MIR182 ; LOC105375501
0.925 0.080 7 129770355 upstream gene variant G/A snv 0.44 0.44
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast 		0.010 1.000 1 2018 2018
dbSNP: rs4541843
rs4541843
MIR182 ; LOC105375501
0.925 0.080 7 129770355 upstream gene variant G/A snv 0.44 0.44
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma 		0.010 1.000 1 2018 2018
dbSNP: rs76481776
rs76481776
MIR182 ; LOC105375501
0.925 0.200 7 129770387 non coding transcript exon variant C/G;T snv 5.9E-02
CUI: C0339573
Disease: Glaucoma, Primary Open Angle
Glaucoma, Primary Open Angle 		0.010 1.000 1 2016 2016
dbSNP: rs76481776
rs76481776
MIR182 ; LOC105375501
0.925 0.200 7 129770387 non coding transcript exon variant C/G;T snv 5.9E-02
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome 		0.010 1.000 1 2014 2014
dbSNP: rs76481776
rs76481776
MIR182 ; LOC105375501
0.925 0.200 7 129770387 non coding transcript exon variant C/G;T snv 5.9E-02
CUI: C0581874
Disease: Late insomnia
Late insomnia 		0.010 1.000 1 2010 2010
dbSNP: rs76481776
rs76481776
MIR182 ; LOC105375501
0.925 0.200 7 129770387 non coding transcript exon variant C/G;T snv 5.9E-02
CUI: C0917801
Disease: Sleeplessness
Sleeplessness 		0.010 1.000 1 2010 2010