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Links from PubMed

Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
MLH1
(Q48E)
Single nucleotide variant
(5 prime UTR variant +2 more)
Hereditary nonpolyposis colorectal neoplasms
+1 more
GUncertain significance
MLH1
(Q48H)
Single nucleotide variant
(5 prime UTR variant +2 more)
Hereditary nonpolyposis colorectal neoplasms
+3 more
GUncertain significance
MLH1
(Q48P)
Single nucleotide variant
(missense variant +2 more)
Lynch syndrome
GLikely pathogenic
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