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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CHRND
(N39K)
Single nucleotide variant
(missense variant +1 more)
Lethal multiple pterygium syndrome
+3 more
GBenign
CHRND
(N130I +3 more)
Single nucleotide variant
(missense variant)
Lethal multiple pterygium syndrome
+1 more
GConflicting classifications of pathogenicity
CHRND
(R244C +2 more)
Single nucleotide variant
(missense variant +1 more)
not provided
+1 more
GConflicting classifications of pathogenicity
CHRND
(L146F +2 more)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
CHRND
(Q288E +3 more)
Single nucleotide variant
(missense variant)
not specified
+3 more
GBenign/Likely benign
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