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: rs3825932
rs3825932
CTSH
0.827 0.360 15 78943104 intron variant T/C snv 0.50
CUI: C0011884
Disease: Diabetic Retinopathy
Diabetic Retinopathy 		0.010 1.000 1 2015 2015
dbSNP: rs3825932
rs3825932
CTSH
0.827 0.360 15 78943104 intron variant T/C snv 0.50
CUI: C1845050
Disease: PIGMENTARY DISORDER, RETICULATE, WITH SYSTEMIC MANIFESTATIONS
PIGMENTARY DISORDER, RETICULATE, WITH SYSTEMIC MANIFESTATIONS 		0.010 1.000 1 2015 2015
dbSNP: rs3825932
rs3825932
CTSH
0.827 0.360 15 78943104 intron variant T/C snv 0.50
CUI: C0154830
Disease: Proliferative diabetic retinopathy
Proliferative diabetic retinopathy 		0.010 1.000 1 2015 2015