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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CRYL1, EEF1AKMT1
+32 more
Duplication
Autosomal recessive nonsyndromic hearing loss 1A
+3 more
GUncertain significance
IL17D, LOC130009328
Single nucleotide variant
(synonymous variant +2 more)
not provided
GLikely benign