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: rs121908012
rs121908012
UROS
3 0.882 0.160 10 125815061 missense variant A/C;G snv 4.0E-06; 2.1E-04 0.010 1.000 1 2013 2013
dbSNP: rs121908021
rs121908021
UROS
2 0.925 0.120 10 125788923 missense variant G/T snv 0.010 1.000 1 2013 2013