List of variants in gene SDCCAG8 reported as likely benign for Bardet-Biedl syndrome 16

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_006642.5(SDCCAG8):c.986C>T (p.Thr329Met)	rs35859404	0.00342
NM_006642.5(SDCCAG8):c.279G>A (p.Pro93=)	rs145877279	0.00120
NM_006642.5(SDCCAG8):c.-4G>A	rs113193158	0.00083
NM_006642.5(SDCCAG8):c.1409A>G (p.Glu470Gly)	rs118064970	0.00062

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