Source: CURATED

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: rs7310615
rs7310615
SH2B3
0.882 12 111427245 intron variant C/G snv 0.67
CUI: C0001948
Disease: Alcohol consumption
Alcohol consumption 		0.700 1.000 2 2018 2019
dbSNP: rs7310615
rs7310615
SH2B3
0.882 12 111427245 intron variant C/G snv 0.67
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 1 2018 2018
dbSNP: rs7310615
rs7310615
SH2B3
0.882 12 111427245 intron variant C/G snv 0.67
CUI: C0004364
Disease: Autoimmune Diseases
Autoimmune Diseases 		0.700 1.000 1 2019 2019
dbSNP: rs7310615
rs7310615
SH2B3
0.882 12 111427245 intron variant C/G snv 0.67
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 1 2019 2019
dbSNP: rs7310615
rs7310615
SH2B3
0.882 12 111427245 intron variant C/G snv 0.67
CUI: C4014795
Disease: AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 1
AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 1 		0.700 1.000 1 2019 2019
dbSNP: rs7310615
rs7310615
SH2B3
0.882 12 111427245 intron variant C/G snv 0.67
CUI: C0337428
Disease: Fibrinogen assay
Fibrinogen assay 		0.700 1.000 1 2016 2016
dbSNP: rs7310615
rs7310615
SH2B3
0.882 12 111427245 intron variant C/G snv 0.67
CUI: C0428886
Disease: Mean blood pressure
Mean blood pressure 		0.700 1.000 1 2018 2018
dbSNP: rs7310615
rs7310615
SH2B3
0.882 12 111427245 intron variant C/G snv 0.67
CUI: C1306620
Disease: Systolic blood pressure measurement
Systolic blood pressure measurement 		0.700 1.000 1 2018 2018
dbSNP: rs7310615
rs7310615
SH2B3
0.882 12 111427245 intron variant C/G snv 0.67
CUI: C3150797
Disease: AUTOIMMUNE DISEASE, SUSCEPTIBILITY TO, 6
AUTOIMMUNE DISEASE, SUSCEPTIBILITY TO, 6 		0.700 1.000 1 2019 2019
dbSNP: rs7310615
rs7310615
SH2B3
0.882 12 111427245 intron variant C/G snv 0.67
CUI: C0202117
Disease: Low density lipoprotein cholesterol measurement
Low density lipoprotein cholesterol measurement 		0.700 1.000 1 2019 2019
dbSNP: rs7310615
rs7310615
SH2B3
0.882 12 111427245 intron variant C/G snv 0.67
CUI: C0428883
Disease: Diastolic blood pressure
Diastolic blood pressure 		0.700 1.000 1 2018 2018
dbSNP: rs7310615
rs7310615
SH2B3
0.882 12 111427245 intron variant C/G snv 0.67
CUI: C4310768
Disease: AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 2
AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 2 		0.700 1.000 1 2019 2019