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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CHSY1, LOC130058068
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
CHSY1, LOC130058068
Single nucleotide variant
(synonymous variant)
not provided
+1 more
GLikely benign
CHSY1, LOC130058068
(N85D)
Single nucleotide variant
(missense variant)
Temtamy preaxial brachydactyly syndrome
+2 more
GUncertain significance
CHSY1, LOC130058068
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
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