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Items: 6

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
EYA4
Single nucleotide variant
(intron variant)
not specified
+3 more
GBenign/Likely benign
EYA4
Single nucleotide variant
(synonymous variant)
Cardiovascular phenotype
+4 more
GConflicting classifications of pathogenicity
EYA4
(M329I +4 more)
Single nucleotide variant
(missense variant)
Cardiovascular phenotype
+4 more
GConflicting classifications of pathogenicity
EYA4
(R345S +4 more)
Single nucleotide variant
(missense variant)
Autosomal dominant nonsyndromic hearing loss 10
+4 more
GConflicting classifications of pathogenicity
EYA4, TARID
Single nucleotide variant
(synonymous variant)
Cardiovascular phenotype
+3 more
GConflicting classifications of pathogenicity
EYA4, TARID
Single nucleotide variant
(synonymous variant)
Autosomal dominant nonsyndromic hearing loss 10
+4 more
GBenign/Likely benign
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