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Items: 36

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
GSR
(D450H +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
GSR
(G469V +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
GSR
(M383V +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
GSR
(G316D +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
GSR
(I304T +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
GSR
(P295L +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
GSR
(T321I +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
GSR
(S293F)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
GSR
(T279M)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
GSR
(N277T)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
GSR
(A252D)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
GSR
(V244E)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
GSR
(V237I)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
GSR
(P231A)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
GSR
(H208Q)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
GSR
(T206P)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
GSR
(T200P)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
GSR
(H166R)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
GSR
(T163I)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
GSR
(Q159L)
Single nucleotide variant
(missense variant)
not specified
+2 more
GUncertain significance
GSR
(R153H)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
GSR
(R147W)
Single nucleotide variant
(missense variant)
not specified
+1 more
GUncertain significance
GSR
(R147G)
Single nucleotide variant
(missense variant)
Hemolytic anemia due to glutathione reductase deficiency
+2 more
GUncertain significance
GSR
(I143T)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
GSR
(K111Q)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
GSR, LOC130000170
(K97R)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
GSR, LOC130000170
(A84T)
Single nucleotide variant
(missense variant)
not provided
+1 more
GConflicting classifications of pathogenicity
GSR, LOC130000170
(R81H)
Single nucleotide variant
(missense variant)
Hemolytic anemia due to glutathione reductase deficiency
+1 more
GUncertain significance
GSR, LOC130000170
(A39T)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
GSR, LOC130000170
(L28P)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
GSR, LOC130000170
(F23V)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
GSR, LOC130000170
(R17Q)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
GSR, LOC130000170
(W16L)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
GSR, LOC130000170
(L8Q)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
GSR, LOC130000170
(A7S)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
GSR, LOC130000170
(R6Q)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
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