List of variants in gene combination ANK1, LOC126860369 reported as uncertain significance for anemia

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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: 4

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HGVS	dbSNP	gnomAD frequency
NM_000037.4(ANK1):c.1800+3A>T	rs559020131	0.00004
NM_000037.4(ANK1):c.1729G>A (p.Val577Ile)
NM_000037.4(ANK1):c.1771C>G (p.Arg591Gly)	rs754903343
NM_000037.4(ANK1):c.1786C>A (p.His596Asn)

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