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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
FREM1
(I1497T +1 more)
Single nucleotide variant
(missense variant +1 more)
Oculotrichoanal syndrome
GUncertain significance
FREM1
(G1357R)
Single nucleotide variant
(missense variant +1 more)
Oculotrichoanal syndrome
+3 more
GConflicting classifications of pathogenicity
FREM1
(G31E)
Single nucleotide variant
(missense variant +1 more)
Oculotrichoanal syndrome
GUncertain significance
FREM1
Single nucleotide variant
(5 prime UTR variant +1 more)
Oculotrichoanal syndrome
+1 more
GConflicting classifications of pathogenicity
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