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: rs104894380
rs104894380
UNG
1 1.000 0.120 12 109103562 missense variant T/C snv 0.800 1.000 2 2003 2005
dbSNP: rs772214871
rs772214871
UNG
1 1.000 0.120 12 109103495 stop gained C/T snv 4.0E-06 2.1E-05 0.700 0