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Links from Gene

Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
MFSD2A
(D106G +3 more)
Single nucleotide variant
(missense variant +3 more)
not provided
GUncertain significance
MFSD2A
(L112P +4 more)
Single nucleotide variant
(missense variant +2 more)
Microcephaly 15, primary, autosomal recessive
GUncertain significance