List of variants reported as pathogenic for holoprosencephaly 2 by OMIM

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Total variants: 8

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HGVS	dbSNP	gnomAD frequency
NM_005413.4(SIX3):c.109G>T (p.Gly37Cys)	rs199823175	0.00210
NM_005413.3(SIX3):c.[206G>A;406_407dup]
NM_005413.4(SIX3):c.339G>T (p.Trp113Cys)	rs137853021
NM_005413.4(SIX3):c.385G>T (p.Glu129Ter)	rs387906867
NM_005413.4(SIX3):c.556_557dup (p.Pro187fs)	rs1572624159
NM_005413.4(SIX3):c.676C>G (p.Leu226Val)	rs121917878
NM_005413.4(SIX3):c.749T>C (p.Val250Ala)	rs121917880
NM_005413.4(SIX3):c.770G>C (p.Arg257Pro)	rs121917879

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