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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
PCSK1, LOC101929710
+1 more
(L713F +1 more)
Single nucleotide variant
(missense variant)
Monogenic Non-Syndromic Obesity
+2 more
GUncertain significance
CAST, LOC101929710
+1 more
(E463K +1 more)
Single nucleotide variant
(missense variant)
Body mass index quantitative trait locus 12
+2 more
GConflicting classifications of pathogenicity
CAST, LOC101929710
+1 more
(Y134H +1 more)
Single nucleotide variant
(missense variant)
Obesity due to prohormone convertase I deficiency
+1 more
GUncertain significance
LOC101929710, PCSK1
+1 more
Single nucleotide variant
(synonymous variant)
not provided
+2 more
GLikely benign
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