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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
MAP2K1
Single nucleotide variant
(intron variant +1 more)
not provided
+2 more
GUncertain significance
MAP2K1
Single nucleotide variant
(intron variant)
Cardiofaciocutaneous syndrome 3
GUncertain significance
MAP2K1, SNAPC5
Microsatellite
(3 prime UTR variant +2 more)
RASopathy
GBenign
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