Gene: SNCG ×
Source: ALL
Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs531523381
rs531523381
SNCG ; MMRN2
1 1.000 0.040 10 86958785 missense variant G/C snv 0.080 1.000 8 1999 2018