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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
HGF
Single nucleotide variant
(intron variant)
HGF-related disorder
+1 more
GLikely benign
HGF
(A46V)
Single nucleotide variant
(missense variant)
Nonsyndromic Hearing Loss, Mixed
+3 more
GConflicting classifications of pathogenicity
HGF
Single nucleotide variant
(synonymous variant)
HGF-related disorder
GLikely benign
HGF
(W2C)
Single nucleotide variant
(missense variant)
HGF-related disorder
+2 more
GConflicting classifications of pathogenicity
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