ClinVar Miner

List of variants in gene AGTR1 reported as likely pathogenic by Institute of Medical Genetics and Applied Genomics, University Hospital Tübingen

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_000685.5(AGTR1):c.500G>A (p.Arg167Gln)	rs200184769	0.00007
NM_000685.5(AGTR1):c.696_700del (p.Pro233fs)	rs2107975487

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