List of variants in gene ALAS2 reported as uncertain significance for hereditary photodermatosis

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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_000032.5(ALAS2):c.661G>A (p.Ala221Thr)	rs753156183	0.00007
NM_000032.5(ALAS2):c.1168+19C>A	rs751844260	0.00001
NM_000032.5(ALAS2):c.1057C>G (p.Leu353Val)	rs1557247532
NM_000032.5(ALAS2):c.1178T>C (p.Phe393Ser)
NM_000032.5(ALAS2):c.1532G>T (p.Arg511Leu)	rs372675935
NM_000032.5(ALAS2):c.1567C>T (p.His523Tyr)	rs199826743
NM_000032.5(ALAS2):c.1651T>G (p.Ser551Ala)

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