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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
MSH6
(I188F)
Single nucleotide variant
(missense variant +2 more)
Hereditary nonpolyposis colorectal neoplasms
+1 more
GUncertain significance
MSH6
(H250P +8 more)
Single nucleotide variant
(missense variant +2 more)
Lynch syndrome 5
GUncertain significance
MSH6
(F958fs +1 more)
Deletion
(frameshift variant)
Lynch syndrome
GPathogenic
MSH6
(R1334Q +2 more)
Single nucleotide variant
(missense variant)
Lynch syndrome
GPathogenic
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