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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
HMCN1, LOC129388665
(T5004F)
Indel
(missense variant)
not specified
+2 more
GBenign/Likely benign
HMCN1, LOC129388665
(T5004S)
Single nucleotide variant
(missense variant)
not specified
+2 more
GBenign/Likely benign
HMCN1, LOC129388665
(T5004I)
Single nucleotide variant
(missense variant)
not specified
+2 more
GBenign/Likely benign
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