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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
DNMT1, LOC126862853
(G1482S +3 more)
Single nucleotide variant
(missense variant)
Hereditary sensory neuropathy-deafness-dementia syndrome
+1 more
GUncertain significance
DNMT1
(H1118R +2 more)
Single nucleotide variant
(missense variant)
not provided
+3 more
GUncertain significance