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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
DHFR, MSH3
(S36C)
Single nucleotide variant
(5 prime UTR variant +2 more)
Hereditary cancer-predisposing syndrome
+1 more
GUncertain significance
DHFR, MSH3
(A61P)
Single nucleotide variant
(5 prime UTR variant +2 more)
not specified
+2 more
GConflicting classifications of pathogenicity