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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
DNMT1
(A1318T +2 more)
Single nucleotide variant
(missense variant)
Hereditary sensory neuropathy-deafness-dementia syndrome
+1 more
GUncertain significance
DNMT1
Single nucleotide variant
(synonymous variant)
not provided
+2 more
GBenign
DNMT1
(H97R)
Single nucleotide variant
(missense variant +1 more)
Hereditary sensory neuropathy-deafness-dementia syndrome
+2 more
GBenign
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