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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
AGTR2
(D41N)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
AGTR2
(K77N)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
AGTR2
(F134fs)
Deletion
(frameshift variant)
not specified
+2 more
GLikely benign
AGTR2
(R248K)
Single nucleotide variant
(missense variant)
AGTR2-related condition
+3 more
GBenign
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