List of variants in gene SASS6 reported as benign for Microcephaly 14, primary, autosomal recessive

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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: 5

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HGVS	dbSNP	gnomAD frequency
NM_194292.3(SASS6):c.776C>T (p.Ala259Val)	rs13375867	0.33090
NM_194292.3(SASS6):c.735A>G (p.Gln245=)	rs150364529	0.00856
NM_194292.3(SASS6):c.312-4A>C	rs149440197	0.00500
NM_194292.3(SASS6):c.1835G>A (p.Arg612His)	rs143522528	0.00356
NM_194292.3(SASS6):c.86G>A (p.Ser29Asn)	rs150589706	0.00001

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