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Items: 8

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ESRRB
(D4E +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
ESRRB
(R6G +1 more)
Single nucleotide variant
(missense variant)
not provided
+2 more
GBenign
ESRRB
(A48V +1 more)
Single nucleotide variant
(missense variant)
ESRRB-related condition
+3 more
GConflicting classifications of pathogenicity
ESRRB
Single nucleotide variant
(synonymous variant)
not provided
+1 more
GConflicting classifications of pathogenicity
ESRRB
Single nucleotide variant
(synonymous variant)
not provided
GUncertain significance
ESRRB
(F456L)
Single nucleotide variant
(3 prime UTR variant +1 more)
not specified
+2 more
GConflicting classifications of pathogenicity
ESRRB
(P480S)
Single nucleotide variant
(3 prime UTR variant +1 more)
not specified
+2 more
GConflicting classifications of pathogenicity
ESRRB
(G499D)
Single nucleotide variant
(3 prime UTR variant +1 more)
not provided
+1 more
GUncertain significance
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