List of variants in gene RNF213 reported as likely pathogenic for intracranial arterial disease

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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: 12

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HGVS	dbSNP	gnomAD frequency
NM_001256071.3(RNF213):c.14429G>A (p.Arg4810Lys)	rs112735431	0.00004
NM_001256071.3(RNF213):c.12037G>A (p.Asp4013Asn)	rs397514563	0.00001
NM_001256071.3(RNF213):c.11986_11989delinsGGGTTAG (p.Pro3996_Cys3997delinsGlyLeuGly)	rs2144460572
NM_001256071.3(RNF213):c.12040C>A (p.His4014Asn)	rs1555675538
NM_001256071.3(RNF213):c.12050G>A (p.Cys4017Tyr)
NM_001256071.3(RNF213):c.12059G>T (p.Cys4020Phe)	rs1599150380
NM_001256071.3(RNF213):c.12341C>G (p.Thr4114Arg)	rs2079442813
NM_001256071.3(RNF213):c.12343_12345del (p.Lys4115del)	rs797045187
NM_001256071.3(RNF213):c.13641-2A>G
NM_001256071.3(RNF213):c.14822T>A (p.Val4941Glu)
NM_001256071.3(RNF213):c.1699A>G (p.Met567Val)
NM_001256071.3(RNF213):c.2875G>T (p.Gly959Ter)	rs546643996

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