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: rs7666265
rs7666265
FAM47E ; FAM47E-STBD1 ; LOC105377286
1.000 0.040 4 76255128 intron variant G/A;T snv
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.700 1.000 1 2011 2011