List of variants in gene RBBP8 reported by CeGaT Center for Human Genetics Tuebingen

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 9

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HGVS	dbSNP	gnomAD frequency
NM_002894.3(RBBP8):c.1766G>A (p.Arg589His)	rs111445733	0.00834
NM_002894.3(RBBP8):c.1644T>C (p.Asp548=)	rs34780140	0.00746
NM_002894.3(RBBP8):c.1367A>G (p.His456Arg)	rs139743319	0.00177
NM_002894.3(RBBP8):c.109+6A>G	rs149189755	0.00083
NM_002894.3(RBBP8):c.1290T>A (p.Thr430=)	rs74565999	0.00029
NM_002894.3(RBBP8):c.1902T>C (p.Cys634=)	rs201620586	0.00004
NM_002894.3(RBBP8):c.726C>T (p.Ser242=)	rs749719024	0.00003
NM_002894.3(RBBP8):c.2481A>C (p.Glu827Asp)
NM_002894.3(RBBP8):c.522C>T (p.Asn174=)

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