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Links from Gene

Items: 12

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LEPR, LEPROT
(R76W +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
LEPR, LEPROT
(I77T +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
LEPR, LEPROT
(V41I +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
LEPR, LEPROT
(V17M +1 more)
Single nucleotide variant
(5 prime UTR variant +1 more)
not specified
GUncertain significance
LEPR, LEPROT
Single nucleotide variant
(intron variant)
not provided
GBenign
LEPR, LEPROT
(L21R +1 more)
Single nucleotide variant
(5 prime UTR variant +1 more)
Obesity due to leptin receptor gene deficiency
GUncertain significance
LEPR, LEPROT
Single nucleotide variant
(5 prime UTR variant)
Obesity due to leptin receptor gene deficiency
GUncertain significance
LEPR, LEPROT
Single nucleotide variant
(synonymous variant +1 more)
not provided
GLikely benign
LEPR, LEPROT
Single nucleotide variant
(5 prime UTR variant +1 more)
not provided
+2 more
GConflicting classifications of pathogenicity
LEPR, LEPROT
Single nucleotide variant
(5 prime UTR variant)
Monogenic Non-Syndromic Obesity
+1 more
GUncertain significance
LEPR, LEPROT
Single nucleotide variant
(5 prime UTR variant)
Monogenic Non-Syndromic Obesity
+1 more
GBenign
LEPR, LEPROT
Single nucleotide variant
(5 prime UTR variant)
Monogenic Non-Syndromic Obesity
+1 more
GUncertain significance
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