List of variants in gene RTN2 reported by CeGaT Center for Human Genetics Tuebingen

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 16

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HGVS	dbSNP	gnomAD frequency
NM_005619.5(RTN2):c.1143G>A (p.Ala381=)	rs45532933	0.00572
NM_005619.5(RTN2):c.444C>G (p.Gly148=)	rs139232850	0.00550
NM_005619.5(RTN2):c.351A>G (p.Gln117=)	rs144028452	0.00450
NM_005619.5(RTN2):c.1168G>A (p.Gly390Ser)	rs143937661	0.00242
NM_005619.5(RTN2):c.560-7G>A	rs370068938	0.00011
NM_005619.5(RTN2):c.939del (p.Thr314fs)	rs768449676	0.00005
NM_005619.5(RTN2):c.986G>A (p.Ser329Asn)	rs145653668	0.00004
NM_005619.5(RTN2):c.1325C>T (p.Ala442Val)	rs201863499	0.00003
NM_005619.5(RTN2):c.461C>T (p.Thr154Met)	rs761153006	0.00002
NM_005619.5(RTN2):c.1181T>G (p.Leu394Arg)	rs755919124	0.00001
NM_005619.5(RTN2):c.1284G>A (p.Thr428=)
NM_005619.5(RTN2):c.1490A>C (p.Gln497Pro)	rs1555797402
NM_005619.5(RTN2):c.265C>T (p.Gln89Ter)	rs1568625691
NM_005619.5(RTN2):c.34+7A>G
NM_005619.5(RTN2):c.37G>T (p.Glu13Ter)	rs1599914870
NM_005619.5(RTN2):c.587A>G (p.Gln196Arg)

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