Source: UNIPROT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs28941474
rs28941474
6 131573314 missense variant T/C snv 4.0E-06 7.0E-06
CUI: C0268548
Disease: Hyperargininemia
Hyperargininemia
0.810 1.000 4 1992 2018
dbSNP: rs104893943
rs104893943
6 131581326 missense variant G/T snv 7.0E-06
CUI: C0268548
Disease: Hyperargininemia
Hyperargininemia
0.800 1.000 4 1992 2013
dbSNP: rs104893948
rs104893948
6 131583392 missense variant G/A;C snv 2.0E-05; 8.0E-06
CUI: C0268548
Disease: Hyperargininemia
Hyperargininemia
0.800 1.000 4 1992 2016