List of variants in gene RNF213 studied for See cases

Minimum submission review status:		Collection method:
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Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 6

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HGVS	dbSNP	gnomAD frequency
NM_001256071.3(RNF213):c.10822G>T (p.Ala3608Ser)
NM_001256071.3(RNF213):c.1112+6G>A	rs1411900717
NM_001256071.3(RNF213):c.11659A>G (p.Lys3887Glu)	rs1555673862
NM_001256071.3(RNF213):c.12028C>G (p.Leu4010Val)
NM_001256071.3(RNF213):c.12858G>T (p.Gln4286His)	rs2144519655
NM_001256071.3(RNF213):c.9649G>A (p.Val3217Ile)

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