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Links from MedGen

Items: 77

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LEP
(P64S)
Single nucleotide variant
(missense variant)
Obesity due to congenital leptin deficiency
GPathogenic
LEP
(G59S)
Single nucleotide variant
(missense variant)
Obesity due to congenital leptin deficiency
GPathogenic
LEP
Single nucleotide variant
(3 prime UTR variant)
Obesity due to congenital leptin deficiency
GUncertain significance
LEP
Single nucleotide variant
(3 prime UTR variant)
Obesity due to congenital leptin deficiency
GUncertain significance
LEP
Single nucleotide variant
(3 prime UTR variant)
Obesity due to congenital leptin deficiency
GUncertain significance
LEP
Single nucleotide variant
(3 prime UTR variant)
Obesity due to congenital leptin deficiency
GUncertain significance
LEP
Single nucleotide variant
(3 prime UTR variant)
Obesity due to congenital leptin deficiency
GUncertain significance
LEP
Single nucleotide variant
(3 prime UTR variant)
Obesity due to congenital leptin deficiency
GUncertain significance
LEP
Single nucleotide variant
(3 prime UTR variant)
Obesity due to congenital leptin deficiency
GUncertain significance
LEP
(A146S)
Single nucleotide variant
(missense variant)
Obesity due to congenital leptin deficiency
GUncertain significance
LEP
Single nucleotide variant
(3 prime UTR variant)
Obesity due to congenital leptin deficiency
GUncertain significance
LEP
Single nucleotide variant
(3 prime UTR variant)
Obesity due to congenital leptin deficiency
GUncertain significance
LEP
Single nucleotide variant
(3 prime UTR variant)
Obesity due to congenital leptin deficiency
GUncertain significance
LEP
Single nucleotide variant
(3 prime UTR variant)
Obesity due to congenital leptin deficiency
GUncertain significance
LEP
Single nucleotide variant
(3 prime UTR variant)
Obesity due to congenital leptin deficiency
GUncertain significance
LEP
Single nucleotide variant
(3 prime UTR variant)
Obesity due to congenital leptin deficiency
GUncertain significance
LEP
Single nucleotide variant
(3 prime UTR variant)
Obesity due to congenital leptin deficiency
GUncertain significance
LEP
(T48M)
Single nucleotide variant
(missense variant)
Obesity due to congenital leptin deficiency
GUncertain significance
LEP
(Y18C)
Single nucleotide variant
(missense variant)
Obesity due to congenital leptin deficiency
+2 more
GConflicting classifications of pathogenicity
LEP
Single nucleotide variant
(3 prime UTR variant)
Obesity due to congenital leptin deficiency
GUncertain significance
LEP
Single nucleotide variant
(3 prime UTR variant)
Obesity due to congenital leptin deficiency
GUncertain significance
LEP
Single nucleotide variant
(3 prime UTR variant)
Obesity due to congenital leptin deficiency
GUncertain significance
LEP
Single nucleotide variant
(3 prime UTR variant)
Obesity due to congenital leptin deficiency
GUncertain significance
LEP
Single nucleotide variant
(3 prime UTR variant)
Obesity due to congenital leptin deficiency
GUncertain significance
LEP
Single nucleotide variant
(3 prime UTR variant)
Obesity due to congenital leptin deficiency
GUncertain significance
LEP
Single nucleotide variant
(5 prime UTR variant)
Obesity due to congenital leptin deficiency
GUncertain significance
LEP
Single nucleotide variant
(3 prime UTR variant)
Obesity due to congenital leptin deficiency
GUncertain significance
LEP
Single nucleotide variant
(3 prime UTR variant)
Obesity due to congenital leptin deficiency
GUncertain significance
LEP
Single nucleotide variant
(3 prime UTR variant)
Obesity due to congenital leptin deficiency
GUncertain significance
LEP
Single nucleotide variant
(3 prime UTR variant)
Obesity due to congenital leptin deficiency
GUncertain significance
LEP
Single nucleotide variant
(synonymous variant)
not provided
+1 more
GConflicting classifications of pathogenicity
LEP
(L154P)
Single nucleotide variant
(missense variant)
Obesity due to congenital leptin deficiency
GLikely pathogenic
LEP
Duplication
(3 prime UTR variant)
Monogenic Non-Syndromic Obesity
+1 more
GUncertain significance
LEP
Duplication
(3 prime UTR variant)
Monogenic Non-Syndromic Obesity
+1 more
GLikely benign
LEP
Duplication
(3 prime UTR variant)
Monogenic Non-Syndromic Obesity
+1 more
GUncertain significance
LEP
Single nucleotide variant
(3 prime UTR variant)
Obesity due to congenital leptin deficiency
+1 more
GUncertain significance
LEP
Single nucleotide variant
(3 prime UTR variant)
Obesity due to congenital leptin deficiency
+1 more
GUncertain significance
LEP
Single nucleotide variant
(3 prime UTR variant)
Obesity due to congenital leptin deficiency
+1 more
GUncertain significance
LEP
Single nucleotide variant
(3 prime UTR variant)
Obesity due to congenital leptin deficiency
+1 more
GLikely benign
LEP
Single nucleotide variant
(3 prime UTR variant)
Obesity due to congenital leptin deficiency
+1 more
GUncertain significance
LEP
Single nucleotide variant
(3 prime UTR variant)
Monogenic Non-Syndromic Obesity
+1 more
GUncertain significance
LEP
Single nucleotide variant
(3 prime UTR variant)
Obesity due to congenital leptin deficiency
+1 more
GBenign/Likely benign
LEP
Single nucleotide variant
(3 prime UTR variant)
Monogenic Non-Syndromic Obesity
+1 more
GUncertain significance
LEP
Single nucleotide variant
(3 prime UTR variant)
Obesity due to congenital leptin deficiency
+1 more
GBenign/Likely benign
LEP
Single nucleotide variant
(3 prime UTR variant)
Monogenic Non-Syndromic Obesity
+1 more
GUncertain significance
LEP
Single nucleotide variant
(3 prime UTR variant)
Obesity due to congenital leptin deficiency
+1 more
GUncertain significance
LEP
Single nucleotide variant
(3 prime UTR variant)
Obesity due to congenital leptin deficiency
+1 more
GLikely benign
LEP
Single nucleotide variant
(3 prime UTR variant)
Obesity due to congenital leptin deficiency
+1 more
GUncertain significance
LEP
Single nucleotide variant
(3 prime UTR variant)
Obesity due to congenital leptin deficiency
+1 more
GUncertain significance
LEP
Single nucleotide variant
(3 prime UTR variant)
Obesity due to congenital leptin deficiency
+1 more
GBenign
LEP
Single nucleotide variant
(3 prime UTR variant)
Obesity due to congenital leptin deficiency
+1 more
GUncertain significance
LEP
Single nucleotide variant
(3 prime UTR variant)
Monogenic Non-Syndromic Obesity
+1 more
GUncertain significance
LEP
Single nucleotide variant
(3 prime UTR variant)
Monogenic Non-Syndromic Obesity
+1 more
GUncertain significance
LEP
Single nucleotide variant
(3 prime UTR variant)
Obesity due to congenital leptin deficiency
+1 more
GUncertain significance
LEP
Single nucleotide variant
(3 prime UTR variant)
Obesity due to congenital leptin deficiency
+1 more
GUncertain significance
LEP
Single nucleotide variant
(3 prime UTR variant)
Obesity due to congenital leptin deficiency
+1 more
GLikely benign
LEP
Single nucleotide variant
(3 prime UTR variant)
Obesity due to congenital leptin deficiency
+1 more
GUncertain significance
LEP
Single nucleotide variant
(3 prime UTR variant)
Obesity due to congenital leptin deficiency
+1 more
GUncertain significance
LEP
Single nucleotide variant
(3 prime UTR variant)
Monogenic Non-Syndromic Obesity
+1 more
GUncertain significance
LEP
Single nucleotide variant
(3 prime UTR variant)
Obesity due to congenital leptin deficiency
+1 more
GUncertain significance
LEP
Single nucleotide variant
(3 prime UTR variant)
Monogenic Non-Syndromic Obesity
+1 more
GUncertain significance
LEP
Single nucleotide variant
(3 prime UTR variant)
Obesity due to congenital leptin deficiency
+1 more
GLikely benign
LEP
Single nucleotide variant
(3 prime UTR variant)
Obesity due to congenital leptin deficiency
+1 more
GUncertain significance
LEP
Single nucleotide variant
(3 prime UTR variant)
Obesity due to congenital leptin deficiency
+1 more
GUncertain significance
LEP
Single nucleotide variant
(3 prime UTR variant)
Monogenic Non-Syndromic Obesity
+1 more
GUncertain significance
LEP
Single nucleotide variant
(3 prime UTR variant)
Monogenic Non-Syndromic Obesity
+1 more
GUncertain significance
LEP
Single nucleotide variant
(3 prime UTR variant)
Monogenic Non-Syndromic Obesity
+1 more
GUncertain significance
LEP
Single nucleotide variant
(3 prime UTR variant)
Monogenic Non-Syndromic Obesity
+1 more
GUncertain significance
LEP
Single nucleotide variant
(3 prime UTR variant)
Monogenic Non-Syndromic Obesity
+2 more
GConflicting classifications of pathogenicity
LEP
(V94M)
Single nucleotide variant
(missense variant)
Obesity due to congenital leptin deficiency
+3 more
GBenign/Likely benign
LEP
(T71N)
Single nucleotide variant
(missense variant)
Monogenic Non-Syndromic Obesity
+1 more
GUncertain significance
LEP
(D61N)
Single nucleotide variant
(missense variant)
Monogenic Non-Syndromic Obesity
+1 more
GUncertain significance
LEP
Single nucleotide variant
(intron variant)
Monogenic Non-Syndromic Obesity
+1 more
GUncertain significance
LEP
Single nucleotide variant
(synonymous variant)
Monogenic Non-Syndromic Obesity
+3 more
GConflicting classifications of pathogenicity
LEP, LOC106728418
Single nucleotide variant
(5 prime UTR variant)
Monogenic Non-Syndromic Obesity
+2 more
GBenign/Likely benign
LEP
(R105W)
Single nucleotide variant
(missense variant)
Obesity due to congenital leptin deficiency
GPathogenic
LEP
(G133fs)
Deletion
(frameshift variant)
Obesity due to congenital leptin deficiency
GPathogenic
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