List of variants in gene RINT1 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: 12

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HGVS	dbSNP	gnomAD frequency
NM_021930.6(RINT1):c.118A>T (p.Ser40Cys)	rs11556986	0.19903
NM_021930.6(RINT1):c.414G>A (p.Ala138=)	rs7805216	0.05199
NM_021930.6(RINT1):c.840-5G>A	rs113947297	0.02620
NM_021930.6(RINT1):c.1374T>C (p.Ala458=)	rs35961194	0.01433
NM_021930.6(RINT1):c.465C>T (p.Ile155=)	rs79893877	0.00636
NM_021930.6(RINT1):c.1025T>C (p.Met342Thr)	rs140651827	0.00073
NM_021930.6(RINT1):c.783G>A (p.Pro261=)	rs144905970	0.00048
NM_021930.6(RINT1):c.1656T>C (p.Asp552=)	rs192297021	0.00013
NM_021930.6(RINT1):c.1870T>C (p.Leu624=)	rs767354831	0.00011
NM_021930.6(RINT1):c.543C>T (p.Thr181=)	rs774063327	0.00004
NM_021930.6(RINT1):c.555G>A (p.Pro185=)	rs187674997	0.00001
NM_021930.6(RINT1):c.43-12TTC[2]	rs374498388

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