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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC130057340, MAP2K1
Microsatellite
(5 prime UTR variant)
Cardio-facio-cutaneous syndrome
+2 more
GLikely benign
LOC130057340, MAP2K1
Duplication
(5 prime UTR variant)
not provided
GLikely benign
LOC130057340, MAP2K1
Single nucleotide variant
(5 prime UTR variant)
not provided
GBenign
LOC130057340, MAP2K1
Single nucleotide variant
(5 prime UTR variant)
not provided
GLikely benign
LOC130057340, MAP2K1
Duplication
not specified
GBenign
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