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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LEPR
(K109R)
Single nucleotide variant
(missense variant)
Monogenic Non-Syndromic Obesity
+3 more
GBenign
LEPR
(P231S)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+1 more
GUncertain significance
LEPR
(K656N)
Single nucleotide variant
(missense variant)
not provided
+3 more
GBenign/Likely benign
LEPR
Single nucleotide variant
(synonymous variant)
Obesity due to leptin receptor gene deficiency
+1 more
GBenign/Likely benign
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