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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
RPL10
Single nucleotide variant
(intron variant)
not specified
GBenign
RPL10
Single nucleotide variant
(synonymous variant)
Inborn genetic diseases
+1 more
GConflicting classifications of pathogenicity
RPL10
Single nucleotide variant
(no sequence alteration)
Inborn genetic diseases
+1 more
GBenign
RPL10
(H213Q +2 more)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
RPL10
(G162S)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
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