List of variants in gene SIX3 reported as likely pathogenic for holoprosencephaly 2

Minimum submission review status:		Collection method:
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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_005413.4(SIX3):c.581G>C (p.Arg194Pro)	rs1666605262
NM_005413.4(SIX3):c.671G>A (p.Trp224Ter)
NM_005413.4(SIX3):c.770G>C (p.Arg257Pro)	rs121917879

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