List of variants in gene GLMN reported as likely pathogenic for cardiovascular disorder

Minimum submission review status:		Collection method:
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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 11

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HGVS	dbSNP	gnomAD frequency
NM_053274.3(GLMN):c.1141-1G>A	rs1375310236	0.00002
NM_053274.3(GLMN):c.1473+2T>A	rs1655201565	0.00001
NM_053274.3(GLMN):c.1083del (p.Thr363fs)	rs1570898051
NM_053274.3(GLMN):c.1323dup (p.Thr442fs)	rs771252983
NM_053274.3(GLMN):c.1355del (p.Leu452fs)	rs773435694
NM_053274.3(GLMN):c.148C>T (p.Gln50Ter)
NM_053274.3(GLMN):c.1585+1G>A
NM_053274.3(GLMN):c.394+1G>A	rs1258933474
NM_053274.3(GLMN):c.465_468del (p.Leu156fs)
NM_053274.3(GLMN):c.554_558delinsG (p.Lys185fs)	rs1570964992
NM_053274.3(GLMN):c.743T>A (p.Leu248Ter)	rs1656251554

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