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: rs104893937
rs104893937
SNCB
4 0.851 0.120 5 176621218 missense variant G/T snv 1.7E-04 2.0E-04 0.010 1.000 1 2007 2007