List of variants in gene SGSH 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: 17

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HGVS	dbSNP	gnomAD frequency
NM_000199.5(SGSH):c.89-45G>A	rs9900509	0.11554
NM_000199.5(SGSH):c.89-39G>A	rs9900502	0.11282
NM_000199.5(SGSH):c.411G>A (p.Ala137=)	rs142557761	0.00230
NM_000199.5(SGSH):c.1283G>A (p.Arg428His)	rs144862290	0.00186
NM_000199.5(SGSH):c.181C>T (p.Arg61Cys)	rs142309764	0.00103
NM_000199.5(SGSH):c.1428C>T (p.His476=)	rs139460639	0.00066
NM_000199.5(SGSH):c.507-7C>T	rs200965114	0.00056
NM_000199.5(SGSH):c.1317C>T (p.Tyr439=)	rs146522699	0.00044
NM_000199.5(SGSH):c.89-4G>A	rs375536965	0.00032
NM_000199.5(SGSH):c.999C>T (p.Tyr333=)	rs149139346	0.00030
NM_000199.5(SGSH):c.397C>A (p.Pro133Thr)	rs199643693	0.00006
NM_000199.5(SGSH):c.1359C>T (p.Thr453=)	rs751980056	0.00005
NM_000199.5(SGSH):c.526G>A (p.Ala176Thr)
NM_000199.5(SGSH):c.658G>T (p.Val220Leu)	rs150508741
NM_000199.5(SGSH):c.664-39_664-38del	rs34029730
NM_000199.5(SGSH):c.90G>A (p.Ala30=)
NM_000199.5(SGSH):c.950-88C>T

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