List of variants in gene combination CARD14, SGSH reported by Genome-Nilou Lab

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: 7

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HGVS	dbSNP	gnomAD frequency
NM_001366385.1(CARD14):c.1852-60T>C	rs2304856	0.51286
NM_001366385.1(CARD14):c.2398+42T>C	rs4889836	0.41735
NM_001366385.1(CARD14):c.2398+30A>G	rs4889996	0.41486
NM_001366385.1(CARD14):c.2398+49G>A	rs4889997	0.40159
NM_001366385.1(CARD14):c.1979-125C>A	rs3813063	0.39591
NM_000199.5(SGSH):c.734G>A (p.Arg245His)	rs104894635	0.00039
NM_001366385.1(CARD14):c.2219+14T>A	rs8069255

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