List of variants in gene MVK reported as benign by ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories

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: 11

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HGVS	dbSNP	gnomAD frequency
NM_000431.4(MVK):c.79-164T>G	rs6606734	0.55050
NM_000431.4(MVK):c.632-18A>G	rs2270375	0.25946
NM_000431.4(MVK):c.510C>T (p.Asp170=)	rs2287218	0.17165
NM_000431.4(MVK):c.769-38C>T	rs35191208	0.16489
NM_000431.4(MVK):c.78+61A>G	rs61940512	0.13119
NM_000431.4(MVK):c.885+24G>A	rs2270374	0.12332
NM_000431.4(MVK):c.371+8C>T	rs67886029	0.05513
NM_000431.4(MVK):c.405G>A (p.Ser135=)	rs34368092	0.05306
NM_000431.4(MVK):c.831C>T (p.Arg277=)	rs104895353	0.01061
NM_000431.4(MVK):c.677+12del	rs774948892
NM_000431.4(MVK):c.780C>A (p.Ile260=)	rs34975996

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