List of variants in gene combination CARD14, SGSH reported as not provided

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: 5

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HGVS	dbSNP	gnomAD frequency
NM_001366385.1(CARD14):c.2044C>T (p.Arg682Trp)	rs117918077	0.01085
NM_000199.5(SGSH):c.734G>A (p.Arg245His)	rs104894635	0.00039
NM_001366385.1(CARD14):c.2140G>A (p.Gly714Ser)	rs151150961	0.00035
NM_001366385.1(CARD14):c.2858C>T (p.Ala953Val)	rs370106410	0.00001
NM_001366385.1(CARD14):c.2919C>G (p.Asp973Glu)	rs144285237

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