"PreventionGenetics, part of Exact Sciences"[submitter] AND "AGTR1"[ge - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3045256	NM_000685.5(AGTR1):c.-47-1034C>T	AGTR1	Single nucleotide variant (5 prime UTR variant +1 more)	AGTR1-related disorder	GLikely benign
Select item 2634148	NM_000685.5(AGTR1):c.-17C>T	AGTR1	Single nucleotide variant (5 prime UTR variant)	AGTR1-related disorder	GUncertain significance
Select item 2630021	NM_000685.5(AGTR1):c.37del (p.Arg13fs)	AGTR1 (R13fs)	Deletion (frameshift variant)	AGTR1-related disorder	GUncertain significance
Select item 343669	NM_000685.5(AGTR1):c.308T>C (p.Ile103Thr)	AGTR1 (I138T +1 more)	Single nucleotide variant (missense variant)	AGTR1-related disorder +2 more	GConflicting classifications of pathogenicity
Select item 3047667	NM_000685.5(AGTR1):c.339C>T (p.Tyr113=)	AGTR1	Single nucleotide variant (synonymous variant)	AGTR1-related disorder	GLikely benign
Select item 256759	NM_000685.5(AGTR1):c.573C>T (p.Leu191=)	AGTR1	Single nucleotide variant (synonymous variant)	Renal tubular dysgenesis +2 more	GBenign
Select item 2635899	NM_000685.5(AGTR1):c.622T>C (p.Phe208Leu)	AGTR1 (F208L)	Single nucleotide variant (missense variant)	AGTR1-related disorder	GUncertain significance
Select item 256758	NM_000685.5(AGTR1):c.1062A>G (p.Pro354=)	AGTR1	Single nucleotide variant (synonymous variant)	not specified +2 more	GBenign

ClinVar