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Links from OMIM

Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
RTTN
(L932F +1 more)
Single nucleotide variant
(missense variant)
MICROCEPHALY, SHORT STATURE, AND POLYMICROGYRIA WITH SEIZURES
GPathogenic
RTTN
(C27Y)
Single nucleotide variant
(5 prime UTR variant +1 more)
not provided
GUncertain significance
IHH
(E95K)
Single nucleotide variant
(missense variant)
not provided
GPathogenic
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