List of variants in gene combination ASTN2, TRIM32 reported as likely benign for Bardet-Biedl syndrome 11

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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_012210.4(TRIM32):c.*692C>G	rs116058338	0.00526
NM_012210.4(TRIM32):c.1222C>T (p.Arg408Cys)	rs3747835	0.00113
NM_012210.4(TRIM32):c.770C>G (p.Thr257Arg)	rs3747834	0.00017

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