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: rs653747
rs653747
LINC00923
15 97659878 intron variant C/T snv 0.48
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		0.010 1.000 1 2017 2017
dbSNP: rs653747
rs653747
LINC00923
15 97659878 intron variant C/T snv 0.48
CUI: C0022658
Disease: Kidney Diseases
Kidney Diseases 		0.010 1.000 1 2017 2017