List of variants in gene HESX1 reported as likely benign 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: 4

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HGVS	dbSNP	gnomAD frequency
NM_003865.3(HESX1):c.374A>G (p.Asn125Ser)	rs9878928	0.07568
NC_000003.12:g.57200194A>C	rs983243	0.00148
NM_003865.3(HESX1):c.385G>A (p.Val129Ile)	rs143057250	0.00064
NM_003865.3(HESX1):c.460-7A>G	rs1579346889

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