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: rs1204919376
rs1204919376
SRGN
3 0.882 0.160 10 69103945 missense variant G/C snv 4.0E-06 0.010 1.000 1 2016 2016