List of variants in gene RBP3 reported as likely pathogenic for perceptual disorders

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: 12

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HGVS	dbSNP	gnomAD frequency
NM_002900.3(RBP3):c.3341G>A (p.Arg1114Gln)	rs201185969	0.00004
NM_002900.3(RBP3):c.509G>A (p.Arg170Gln)	rs782671340	0.00004
NM_002900.3(RBP3):c.2523C>G (p.Tyr841Ter)	rs781881541	0.00001
NM_002900.3(RBP3):c.1237C>T (p.Pro413Ser)	rs782469310
NM_002900.3(RBP3):c.1408del (p.Asp470fs)	rs1836931186
NM_002900.3(RBP3):c.1472del (p.Leu491fs)
NM_002900.3(RBP3):c.1682_1686dup (p.Thr563fs)	rs1555211286
NM_002900.3(RBP3):c.249C>A (p.Asn83Lys)	rs782215106
NM_002900.3(RBP3):c.2971_2973del (p.Met991del)
NM_002900.3(RBP3):c.3087C>T (p.Ile1029=)
NM_002900.3(RBP3):c.3459G>C (p.Glu1153Asp)
NM_002900.3(RBP3):c.826TTC[2] (p.Phe278del)	rs782604129

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