List of variants in gene combination HOXA1, HOXA2 reported as likely benign for Human HOXA1 syndromes

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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: 3

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HGVS	dbSNP	gnomAD frequency
NM_006735.4(HOXA2):c.*108C>T	rs117630421	0.03326
NM_005522.5(HOXA1):c.213C>T (p.His71=)	rs2074398	0.02428
NM_005522.5(HOXA1):c.436C>A (p.His146Asn)	rs45571645	0.01487

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