List of variants in gene AAAS reported as likely benign for triple-A syndrome

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 7

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HGVS	dbSNP	gnomAD frequency
NM_015665.6(AAAS):c.414T>C (p.Asp138=)	rs11540353	0.07449
NM_015665.6(AAAS):c.1557T>C (p.Thr519=)	rs112987708	0.02027
NM_015665.6(AAAS):c.1515T>C (p.Pro505=)	rs35282133	0.00843
NM_015665.6(AAAS):c.1597G>A (p.Gly533Arg)	rs34451260	0.00840
NM_015665.5(AAAS):c.*32C>T	rs138994144	0.00246
NM_015665.6(AAAS):c.327G>T (p.Thr109=)	rs190876509	0.00038
NM_015665.6(AAAS):c.234G>A (p.Lys78=)	rs145519240	0.00002

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