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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC130055766, SIX1
Single nucleotide variant
(5 prime UTR variant)
Autosomal dominant nonsyndromic hearing loss 23
+1 more
GUncertain significance
LOC130055766, SIX1
Single nucleotide variant
(5 prime UTR variant)
Autosomal dominant nonsyndromic hearing loss 23
+1 more
GUncertain significance
LOC130055766, SIX1
Single nucleotide variant
(5 prime UTR variant)
Nonsyndromic Hearing Loss, Dominant
+1 more
GLikely benign
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