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Links from Gene

Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CNP, DNAJC7
(G419S +1 more)
Single nucleotide variant
(3 prime UTR variant +2 more)
not specified
GUncertain significance
CNP, DNAJC7
(G487R +1 more)
Single nucleotide variant
(3 prime UTR variant +2 more)
not specified
GUncertain significance
CNP, DNAJC7
Single nucleotide variant
(3 prime UTR variant +1 more)
not provided
GBenign
CNP, LOC130060859
Single nucleotide variant
(5 prime UTR variant)
Myopia 2, autosomal dominant
GPathogenic
CNP, LOC130060859
Single nucleotide variant
(5 prime UTR variant)
Myopia 2, autosomal dominant
GPathogenic
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