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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
AGTR2
Single nucleotide variant
(synonymous variant)
AGTR2-related condition
+1 more
GBenign/Likely benign
AGTR2
(F134fs)
Deletion
(frameshift variant)
not provided
+2 more
GLikely benign
AGTR2
(C169F)
Single nucleotide variant
(missense variant)
AGTR2-related condition
GUncertain significance
AGTR2
(R248K)
Single nucleotide variant
(missense variant)
AGTR2-related condition
+2 more
GBenign
AGTR2
(R324Q)
Single nucleotide variant
(missense variant)
AGTR2-related condition
GLikely benign
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