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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC125467768, PCDH19
Single nucleotide variant
(synonymous variant)
not provided
GUncertain significance
LOC125467768, PCDH19
(R794H +1 more)
Single nucleotide variant
(missense variant)
not provided
+1 more
GConflicting classifications of pathogenicity
LOC125467768, PCDH19
Single nucleotide variant
(synonymous variant)
not specified
+2 more
GConflicting classifications of pathogenicity
LOC125467768, PCDH19
Single nucleotide variant
(synonymous variant)
Inborn genetic diseases
+3 more
GBenign/Likely benign
LOC125467768, PCDH19
(R791Q +1 more)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
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