List of variants in gene combination LOC130003079, MAN1B1 reported as likely benign for Rafiq syndrome

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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_016219.5(MAN1B1):c.219+16G>C	rs748529006	0.00001
NM_016219.5(MAN1B1):c.219+20G>A	rs561406012	0.00001
NM_016219.5(MAN1B1):c.219+9C>A	rs749511040	0.00001
NM_016219.5(MAN1B1):c.159G>A (p.Thr53=)	rs774835139
NM_016219.5(MAN1B1):c.219+13C>T	rs774677511

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