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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LEPR, LOC122094844
(S675T)
Single nucleotide variant
(missense variant)
LEPR-related disorder
GUncertain significance
LEPR, LOC122094844
(R678S)
Single nucleotide variant
(missense variant)
not specified
+2 more
GUncertain significance
LEPR, LOC122094844
Single nucleotide variant
(synonymous variant)
LEPR-related disorder
+1 more
GConflicting classifications of pathogenicity
LEPR, LOC122094844
(V724A)
Single nucleotide variant
(missense variant)
not provided
+3 more
GConflicting classifications of pathogenicity
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