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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
NR2F1, NR2F1-AS1
(A2V)
Single nucleotide variant
(missense variant)
Bosch-Boonstra-Schaaf optic atrophy syndrome
GUncertain significance
NR2F1, NR2F1-AS1
Single nucleotide variant
(synonymous variant)
Bosch-Boonstra-Schaaf optic atrophy syndrome
GUncertain significance
NR2F1, NR2F1-AS1
(P58H)
Single nucleotide variant
(missense variant)
Bosch-Boonstra-Schaaf optic atrophy syndrome
GUncertain significance
NR2F1, NR2F1-AS1
(F109L)
Single nucleotide variant
(missense variant)
Bosch-Boonstra-Schaaf optic atrophy syndrome
GLikely pathogenic
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