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: rs1049334
rs1049334
CAV1
0.851 0.280 7 116560326 3 prime UTR variant G/A;T snv
CUI: C0004238
Disease: Atrial Fibrillation
Atrial Fibrillation 		0.700 1.000 1 2017 2017
dbSNP: rs1049334
rs1049334
CAV1
0.851 0.280 7 116560326 3 prime UTR variant G/A;T snv
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms 		0.010 1.000 1 2019 2019
dbSNP: rs1049334
rs1049334
CAV1
0.851 0.280 7 116560326 3 prime UTR variant G/A;T snv
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm 		0.010 1.000 1 2019 2019
dbSNP: rs1049334
rs1049334
CAV1
0.851 0.280 7 116560326 3 prime UTR variant G/A;T snv
CUI: C0279702
Disease: Conventional (Clear Cell) Renal Cell Carcinoma
Conventional (Clear Cell) Renal Cell Carcinoma 		0.010 1.000 1 2015 2015
dbSNP: rs1049334
rs1049334
CAV1
0.851 0.280 7 116560326 3 prime UTR variant G/A;T snv
CUI: C0019163
Disease: Hepatitis B
Hepatitis B 		0.010 1.000 1 2017 2017
dbSNP: rs1049334
rs1049334
CAV1
0.851 0.280 7 116560326 3 prime UTR variant G/A;T snv
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma 		0.010 1.000 1 2017 2017