List of variants in gene GALC reported as benign by Mayo Clinic Laboratories, Mayo Clinic

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: 16

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HGVS	dbSNP	gnomAD frequency
NM_000153.4(GALC):c.1698A>T (p.Val566=)	rs421466	0.95773
NM_000153.4(GALC):c.1834+5C>G	rs448805	0.95475
NM_000153.4(GALC):c.1921A>G (p.Thr641Ala)	rs421262	0.95462
NM_000153.4(GALC):c.1671-15C>T	rs12432149	0.45011
NM_000153.4(GALC):c.1350C>T (p.Ser450=)	rs398076	0.39907
NM_000153.4(GALC):c.984G>A (p.Gln328=)	rs12888666	0.29819
NM_000153.4(GALC):c.328+19T>A	rs74337989	0.12002
NM_000153.4(GALC):c.621+24T>C	rs45568734	0.11420
NM_000153.4(GALC):c.42G>C (p.Ala14=)	rs112992946	0.11300
NM_000153.4(GALC):c.61G>C (p.Ala21Pro)	rs111887056	0.11296
NM_000153.4(GALC):c.75C>A (p.Gly25=)	rs111976362	0.11287
NM_000153.4(GALC):c.330C>T (p.Asp110=)	rs11552556	0.03162
NM_000153.4(GALC):c.1338+23T>C	rs74076317	0.01816
NM_000153.4(GALC):c.1072C>T (p.Leu358=)	rs74073730	0.01792
NM_000153.4(GALC):c.1162-4del	rs11300320
NM_000153.4(GALC):c.196-3del	rs561184126

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