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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
RFT1
Single nucleotide variant
(synonymous variant)
RFT1-related condition
+2 more
GBenign
RFT1
(A463V)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+2 more
GUncertain significance
RFT1
Single nucleotide variant
(intron variant)
RFT1-related condition
+2 more
GConflicting classifications of pathogenicity
RFT1
(L128F)
Single nucleotide variant
(missense variant)
not provided
+1 more
GConflicting classifications of pathogenicity
RFT1
(V46I)
Single nucleotide variant
(missense variant)
not provided
+1 more
GConflicting classifications of pathogenicity
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