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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
DIAPH1
Microsatellite
(inframe_insertion)
Autosomal dominant nonsyndromic hearing loss 1
+3 more
GBenign/Likely benign
DIAPH1
(P620del +1 more)
Microsatellite
(inframe_deletion)
not specified
+3 more
GBenign
DIAPH1
Single nucleotide variant
(intron variant)
not specified
+3 more
GBenign
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