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: rs121908491
rs121908491
SGCE ; CASD1
1 1.000 0.040 7 94618833 missense variant A/C snv 0.800 1.000 11 2001 2011