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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SERPINB6
(G322R +4 more)
Single nucleotide variant
(missense variant +1 more)
Autosomal recessive nonsyndromic hearing loss 91
+2 more
GUncertain significance
SERPINB6
(T88M +4 more)
Single nucleotide variant
(missense variant +1 more)
not provided
+2 more
GUncertain significance