List of variants in gene RIPOR2 reported as benign for not specified

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: 27

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HGVS	dbSNP	gnomAD frequency
NM_001286445.3(RIPOR2):c.2811T>C (p.Ser937=)	rs9358804	0.74640
NM_001286445.3(RIPOR2):c.*7G>A	rs9358799	0.44982
NM_001286445.3(RIPOR2):c.2937T>C (p.Ala979=)	rs9358802	0.29439
NM_001286445.3(RIPOR2):c.2540G>A (p.Arg847Gln)	rs9461073	0.24950
NM_001286445.3(RIPOR2):c.3043+9T>A	rs9379693	0.12477
NM_001286445.3(RIPOR2):c.2895A>G (p.Leu965=)	rs61733143	0.03439
NM_001286445.3(RIPOR2):c.1207G>A (p.Glu403Lys)	rs34016544	0.03314
NM_001286445.3(RIPOR2):c.1495C>T (p.Arg499Cys)	rs35780910	0.03306
NM_001286445.3(RIPOR2):c.1292C>G (p.Ser431Cys)	rs34298086	0.02703
NM_001286445.3(RIPOR2):c.2581G>A (p.Val861Ile)	rs61741706	0.02466
NM_001286445.3(RIPOR2):c.521C>G (p.Ala174Gly)	rs11967003	0.02425
NM_001286445.3(RIPOR2):c.1164+402C>G	rs74477879	0.02339
NM_001286445.3(RIPOR2):c.1086A>G (p.Ala362=)	rs35698586	0.02330
NM_001286445.3(RIPOR2):c.1420G>A (p.Glu474Lys)	rs35514577	0.02169
NM_001286445.3(RIPOR2):c.1072G>T (p.Ala358Ser)	rs35254980	0.02121
NM_001286445.3(RIPOR2):c.2507-6G>A	rs144190405	0.01260
NM_001286445.3(RIPOR2):c.715+8T>C	rs35730227	0.00970
NM_001286445.3(RIPOR2):c.1045G>A (p.Val349Met)	rs35331811	0.00913
NM_001286445.3(RIPOR2):c.3044-12T>C	rs115680381	0.00627
NM_001286445.3(RIPOR2):c.1613C>T (p.Ser538Leu)	rs142889670	0.00401
NM_001286445.3(RIPOR2):c.1850T>G (p.Ile617Ser)	rs115013548	0.00401
NM_001286445.3(RIPOR2):c.1773A>C (p.Leu591Phe)	rs143785002	0.00396
NM_001286445.3(RIPOR2):c.1716T>C (p.Ser572=)	rs148527955	0.00394
NM_001286445.3(RIPOR2):c.1452A>G (p.Pro484=)	rs151067857	0.00380
NM_001286445.3(RIPOR2):c.1397G>A (p.Arg466Lys)	rs142328958	0.00379
NM_001286445.3(RIPOR2):c.1764T>C (p.Asn588=)	rs145837095	0.00378
NM_001286445.3(RIPOR2):c.114G>C (p.Ser38=)	rs2295197

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