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: rs531523381
rs531523381
SNCG ; MMRN2
1.000 0.040 10 86958785 missense variant G/C snv
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.080 1.000 8 1999 2018