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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CHRND
Single nucleotide variant
(synonymous variant +1 more)
Lethal multiple pterygium syndrome
+3 more
GLikely benign
CHRND
(D186N +2 more)
Single nucleotide variant
(missense variant +1 more)
Lethal multiple pterygium syndrome
+3 more
GUncertain significance
CHRND
(R243C +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
+6 more
GConflicting classifications of pathogenicity
CHRND
(P307S +3 more)
Single nucleotide variant
(missense variant)
not provided
+5 more
GConflicting classifications of pathogenicity
CHRND
(R407Q +3 more)
Single nucleotide variant
(missense variant)
Lethal multiple pterygium syndrome
+4 more
GUncertain significance
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