List of variants in gene SIX1 reported as benign for Branchiootic syndrome 3

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: 19

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HGVS	dbSNP	gnomAD frequency
NM_005982.4(SIX1):c.*334C>G	rs10144415	0.83338
NM_005982.4(SIX1):c.*602G>C	rs78909843	0.02638
NM_005982.4(SIX1):c.*404A>G	rs76116881	0.02596
NM_005982.4(SIX1):c.*1496C>T	rs61993831	0.00969
NM_005982.4(SIX1):c.*297T>G	rs147081368	0.00707
NM_005982.4(SIX1):c.-137C>T	rs139621918	0.00654
NM_005982.4(SIX1):c.-184A>C	rs187402923	0.00127
NM_005982.4(SIX1):c.330G>A (p.Arg110=)	rs73309461	0.00078
NM_005982.4(SIX1):c.*443A>G	rs186530769	0.00053
NM_005982.4(SIX1):c.578A>T (p.Asn193Ile)	rs142301715	0.00032
NM_005982.4(SIX1):c.-14G>T	rs374228886	0.00031
NM_005982.4(SIX1):c.162G>A (p.Ala54=)	rs150550985	0.00031
NM_005982.4(SIX1):c.*1079T>A	rs559116477	0.00024
NM_005982.4(SIX1):c.679G>T (p.Asp227Tyr)	rs144481204	0.00018
NM_005982.4(SIX1):c.*1044G>T	rs3742637	0.00014
NM_005982.4(SIX1):c.180C>G (p.Arg60=)	rs781519092	0.00011
NM_005982.4(SIX1):c.-121C>G	rs375002099	0.00010
NM_005982.4(SIX1):c.-24C>T	rs201700039	0.00005
NM_005982.4(SIX1):c.561-34_561-31del	rs34899649

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