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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
AMER1
(S1110T)
Single nucleotide variant
(missense variant)
Osteopathia striata with cranial sclerosis
GUncertain significance
AMER1
(C788Y)
Single nucleotide variant
(missense variant)
Osteopathia striata with cranial sclerosis
GUncertain significance
AMER1
(Y526fs)
Deletion
(frameshift variant)
Osteopathia striata with cranial sclerosis
GLikely pathogenic
AMER1
Single nucleotide variant
(synonymous variant)
Osteopathia striata with cranial sclerosis
GUncertain significance
AMER1
(T24I)
Single nucleotide variant
(missense variant)
Osteopathia striata with cranial sclerosis
GUncertain significance
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