Source: GWASDB

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: rs10069690
rs10069690
0.595 0.560 5 1279675 intron variant C/T snv 0.36
CUI: C0023434
Disease: Chronic Lymphocytic Leukemia
Chronic Lymphocytic Leukemia
0.800 1.000 1 2013 2019
dbSNP: rs10069690
rs10069690
0.595 0.560 5 1279675 intron variant C/T snv 0.36
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast
0.750 1.000 3 2011 2019
dbSNP: rs10069690
rs10069690
0.595 0.560 5 1279675 intron variant C/T snv 0.36
CUI: C0206062
Disease: Lung Diseases, Interstitial
Lung Diseases, Interstitial
0.700 1.000 1 2013 2013
dbSNP: rs10069690
rs10069690
0.595 0.560 5 1279675 intron variant C/T snv 0.36
Malignant Testicular Germ Cell Tumor
0.700 1.000 1 2010 2010