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: rs1553260624
rs1553260624
H3-3A
0.763 0.080 1 226064454 missense variant G/A snv
CUI: C0017636
Disease: Glioblastoma
Glioblastoma 		0.040 1.000 4 2013 2017
dbSNP: rs1553260624
rs1553260624
H3-3A
0.763 0.080 1 226064454 missense variant G/A snv
CUI: C1621958
Disease: Glioblastoma Multiforme
Glioblastoma Multiforme 		0.020 1.000 2 2013 2013
dbSNP: rs1553260624
rs1553260624
H3-3A
0.763 0.080 1 226064454 missense variant G/A snv
CUI: C0027651
Disease: Neoplasms
Neoplasms 		0.020 1.000 2 2012 2017
dbSNP: rs1553260624
rs1553260624
H3-3A
0.763 0.080 1 226064454 missense variant G/A snv
CUI: C0017638
Disease: Glioma
Glioma 		0.010 1.000 1 2019 2019
dbSNP: rs1553260624
rs1553260624
H3-3A
0.763 0.080 1 226064454 missense variant G/A snv
CUI: C0555198
Disease: Malignant Glioma
Malignant Glioma 		0.010 1.000 1 2019 2019
dbSNP: rs1553260624
rs1553260624
H3-3A
0.763 0.080 1 226064454 missense variant G/A snv
CUI: C0029463
Disease: Osteosarcoma
Osteosarcoma 		0.010 1.000 1 2017 2017
dbSNP: rs1553260624
rs1553260624
H3-3A
0.763 0.080 1 226064454 missense variant G/A snv
CUI: C0334587
Disease: Astroblastoma
Astroblastoma 		0.010 1.000 1 2017 2017
dbSNP: rs1553260624
rs1553260624
H3-3A
0.763 0.080 1 226064454 missense variant G/A snv
CUI: C4722099
Disease: High grade glioma
High grade glioma 		0.010 1.000 1 2019 2019
dbSNP: rs1553260624
rs1553260624
H3-3A
0.763 0.080 1 226064454 missense variant G/A snv
CUI: C0206638
Disease: Giant Cell Tumor of Bone
Giant Cell Tumor of Bone 		0.010 1.000 1 2018 2018
dbSNP: rs1553260624
rs1553260624
H3-3A
0.763 0.080 1 226064454 missense variant G/A snv
CUI: C0206064
Disease: Microvascular Angina
Microvascular Angina 		0.010 1.000 1 2012 2012
dbSNP: rs1553260624
rs1553260624
H3-3A
0.763 0.080 1 226064454 missense variant G/A snv
CUI: C0027627
Disease: Neoplasm Metastasis
Neoplasm Metastasis 		0.010 1.000 1 2019 2019
dbSNP: rs1553260624
rs1553260624
H3-3A
0.763 0.080 1 226064454 missense variant G/A snv
CUI: C2939419
Disease: Secondary Neoplasm
Secondary Neoplasm 		0.010 1.000 1 2019 2019
dbSNP: rs1553260624
rs1553260624
H3-3A
0.763 0.080 1 226064454 missense variant G/A snv
CUI: C0206715
Disease: Neoplasms, Neuroepithelial
Neoplasms, Neuroepithelial 		0.010 1.000 1 2019 2019