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Items: 12

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
GHRL, GHRLOS
(I104N +4 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
GHRL, GHRLOS
(H43D +4 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
GHRL, GHRLOS
(V77I +4 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
GHRL, GHRLOS
(F68S +4 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
GHRL, GHRLOS
(A56S +3 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
GHRL, GHRLOS
(P46L +3 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
GHRL, GHRLOS
(R57H +3 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GLikely benign
GHRL, GHRLOS
(W43L +3 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
GHRL, GHRLOS
(Q36R)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
GHRL, GHRLOS
(R34T)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
GHRL, GHRLOS
(L28P)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
GHRL, GHRLOS
+1 more
(V23I)
Single nucleotide variant
(non-coding transcript variant +2 more)
not specified
GUncertain significance
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