List of variants in gene RAX2 reported as benign for not provided

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: 13

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HGVS	dbSNP	gnomAD frequency
NM_001319074.4(RAX2):c.*866C>T	rs917545	0.78969
NM_001319074.4(RAX2):c.*1366C>G	rs6510769	0.25783
NM_001319074.4(RAX2):c.*785G>A	rs917546	0.20551
NM_001319074.4(RAX2):c.*720G>A	rs917547	0.16734
NM_001319074.4(RAX2):c.*1149C>T	rs1860322	0.15969
NM_001319074.4(RAX2):c.217-8C>T	rs79588413	0.15214
NM_001319074.4(RAX2):c.155C>T (p.Pro52Leu)	rs76076446	0.01485
NM_001319074.4(RAX2):c.*381A>G	rs73531473	0.01319
NM_001319074.4(RAX2):c.45T>G (p.Gly15=)	rs139127905	0.00435
NM_001319074.4(RAX2):c.432G>A (p.Ala144=)	rs149918940	0.00108
NM_001319074.4(RAX2):c.282C>T (p.Ala94=)	rs201021639	0.00102
NM_001319074.4(RAX2):c.345G>A (p.Ser115=)	rs755282511	0.00007
NM_001319074.4(RAX2):c.216+15del	rs1034522582

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