Source: CLINVAR

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: rs80358807
rs80358807
0.763 0.280 13 32340146 stop gained C/T snv
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast
0.710 1.000 0 2017 2017
dbSNP: rs80358807
rs80358807
0.763 0.280 13 32340146 stop gained C/T snv
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
0.700 1.000 1 2005 2005
dbSNP: rs80358807
rs80358807
0.763 0.280 13 32340146 stop gained C/T snv
CUI: C2751641
Disease: GLIOMA SUSCEPTIBILITY 3
GLIOMA SUSCEPTIBILITY 3
0.700 0
dbSNP: rs80358807
rs80358807
0.763 0.280 13 32340146 stop gained C/T snv
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate
0.700 0
dbSNP: rs80358807
rs80358807
0.763 0.280 13 32340146 stop gained C/T snv
CUI: C0025149
Disease: Medulloblastoma
Medulloblastoma
0.700 0
dbSNP: rs80358807
rs80358807
0.763 0.280 13 32340146 stop gained C/T snv
BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 2
0.700 0
dbSNP: rs80358807
rs80358807
0.763 0.280 13 32340146 stop gained C/T snv
FANCONI ANEMIA, COMPLEMENTATION GROUP D1
0.700 0
dbSNP: rs80358807
rs80358807
0.763 0.280 13 32340146 stop gained C/T snv
PANCREATIC CANCER, SUSCEPTIBILITY TO, 2
0.700 0
dbSNP: rs80358807
rs80358807
0.763 0.280 13 32340146 stop gained C/T snv
CUI: C0027708
Disease: Nephroblastoma
Nephroblastoma
0.700 0