List of variants in gene MMP21 reported by GeneDx

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: 17

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HGVS	dbSNP	gnomAD frequency
NM_147191.1(MMP21):c.264G>A (p.Ala88=)	rs28381281	0.32198
NM_147191.1(MMP21):c.1203G>A (p.Trp401Ter)	rs137955225	0.00027
NM_147191.1(MMP21):c.1372C>T (p.Arg458Ter)	rs145119918	0.00016
NM_147191.1(MMP21):c.643G>A (p.Glu215Lys)	rs145789868	0.00013
NM_147191.1(MMP21):c.1358C>T (p.Thr453Met)	rs377123310	0.00007
NM_147191.1(MMP21):c.1223G>A (p.Arg408His)	rs372562000	0.00003
NM_147191.1(MMP21):c.356T>G (p.Val119Gly)	rs1251807420	0.00003
NM_147191.1(MMP21):c.736G>A (p.Gly246Arg)	rs746583239	0.00003
NM_147191.1(MMP21):c.832C>G (p.Leu278Val)	rs372964808	0.00003
NM_147191.1(MMP21):c.1025_1026del (p.Lys342fs)	rs1487834487
NM_147191.1(MMP21):c.1198A>G (p.Ile400Val)
NM_147191.1(MMP21):c.1539T>G (p.Tyr513Ter)	rs948481222
NM_147191.1(MMP21):c.240dup (p.Lys81fs)	rs886041273
NM_147191.1(MMP21):c.430C>A (p.Arg144Ser)
NM_147191.1(MMP21):c.536G>C (p.Arg179Pro)
NM_147191.1(MMP21):c.653C>G (p.Ala218Gly)	rs1850480795
NM_147191.1(MMP21):c.793C>G (p.His265Asp)	rs1850462875

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