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: rs759870075
rs759870075
CHST6
1 1.000 0.080 16 75479218 missense variant G/C;T snv 8.3E-06 0.700 1.000 17 2000 2015