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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
COL4A6
(G836S +2 more)
Single nucleotide variant
(missense variant)
Hearing loss, X-linked 6
GUncertain significance
COL4A6
(G210R +1 more)
Single nucleotide variant
(missense variant)
Hearing loss, X-linked 6
GUncertain significance
COL4A6
(S25F +1 more)
Single nucleotide variant
(missense variant)
Hearing loss, X-linked 6
GUncertain significance
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