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: rs17621345
rs17621345
SUGCT
1 1.000 0.080 7 40835593 intron variant A/C snv 0.21 0.700 1.000 1 2018 2018