List of variants in gene combination CRYGD, LOC100507443 reported as likely benign by PreventionGenetics, part of Exact Sciences

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: 6

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HGVS	dbSNP	gnomAD frequency
NM_006891.4(CRYGD):c.168C>G (p.Tyr56Ter)	rs202233735	0.00627
NM_006891.4(CRYGD):c.376G>A (p.Val126Met)	rs150318966	0.00220
NM_006891.4(CRYGD):c.189T>C (p.Tyr63=)	rs200911604	0.00004
NM_006891.4(CRYGD):c.19T>C (p.Tyr7His)
NM_006891.4(CRYGD):c.253-5G>A
NM_006891.4(CRYGD):c.279T>C (p.Tyr93=)

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