SLC7A2, solute carrier family 7 member 2, 6542

N. diseases: 30; N. variants: 4
Disease: Amino acids measurement ×
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs56335308
rs56335308 		8 17561952 missense variant G/A snv 1.8E-02 1.6E-02
CUI: C0201874
Disease: Amino acids measurement
Amino acids measurement 		0.700 1.000 1 2019 2019
dbSNP: rs7838611
rs7838611 		8 17565208 3 prime UTR variant A/G snv 0.12
CUI: C0201874
Disease: Amino acids measurement
Amino acids measurement 		0.700 1.000 1 2019 2019