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Items: 10

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
RGR
Single nucleotide variant
(synonymous variant)
not provided
+3 more
GBenign
RGR
Single nucleotide variant
(synonymous variant)
not specified
+4 more
GBenign
RGR
(A61V)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
RGR
(S66R)
Single nucleotide variant
(missense variant)
not provided
+2 more
GConflicting classifications of pathogenicity
RGR
(R79I +1 more)
Indel
(missense variant)
not provided
GUncertain significance
RGR
Single nucleotide variant
(synonymous variant)
not specified
+2 more
GConflicting classifications of pathogenicity
RGR
(V133I +1 more)
Single nucleotide variant
(missense variant)
Retinitis pigmentosa
+1 more
GUncertain significance
RGR
Single nucleotide variant
(synonymous variant)
not specified
+4 more
GBenign
RGR
(L193V +1 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+1 more
GUncertain significance
RGR
Single nucleotide variant
(intron variant)
RGR-related condition
+4 more
GConflicting classifications of pathogenicity
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