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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
MSH6
(V878A +2 more)
Single nucleotide variant
(missense variant)
Lynch syndrome
GBenign
MSH6
(T1243S +2 more)
Single nucleotide variant
(missense variant)
Inherited ovarian cancer (without breast cancer)
+6 more
GConflicting classifications of pathogenicity