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: rs4629571
rs4629571
HMGCR ; CERT1
0.925 0.160 5 75362479 intron variant A/G snv 8.7E-02
CUI: C0020459
Disease: Hyperinsulinism
Hyperinsulinism 		0.010 1.000 1 2010 2010
dbSNP: rs4629571
rs4629571
HMGCR ; CERT1
0.925 0.160 5 75362479 intron variant A/G snv 8.7E-02
CUI: C0032460
Disease: Polycystic Ovary Syndrome
Polycystic Ovary Syndrome 		0.010 1.000 1 2010 2010