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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LHFPL5
Single nucleotide variant
(3 prime UTR variant)
Autosomal recessive nonsyndromic hearing loss 67
GUncertain significance
LHFPL5
Single nucleotide variant
(3 prime UTR variant)
Autosomal recessive nonsyndromic hearing loss 67
GUncertain significance
LHFPL5
Single nucleotide variant
(3 prime UTR variant)
Autosomal recessive nonsyndromic hearing loss 67
GUncertain significance
LHFPL5
Single nucleotide variant
(3 prime UTR variant)
not provided
+1 more
GUncertain significance
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