List of variants in gene HESX1 reported as likely pathogenic for Septo-optic dysplasia sequence

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)
		ClinVar version:

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_003865.3(HESX1):c.475C>T (p.Arg159Trp)	rs770886420	0.00004
NM_003865.3(HESX1):c.349C>T (p.Gln117Ter)
NM_003865.3(HESX1):c.3G>A (p.Met1Ile)	rs2107566038

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