List of variants in gene GALC reported as benign for not specified

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: 29

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HGVS	dbSNP	gnomAD frequency
NM_000153.4(GALC):c.1620A>G (p.Thr540=)	rs367327	0.95828
NM_000153.4(GALC):c.1698A>T (p.Val566=)	rs421466	0.95773
NM_000153.4(GALC):c.1834+5C>G	rs448805	0.95701
NM_000153.4(GALC):c.1921A>G (p.Thr641Ala)	rs421262	0.95687
NM_000153.4(GALC):c.196-43C>T	rs2289511	0.59150
NM_000153.4(GALC):c.1685T>C (p.Ile562Thr)	rs398607	0.49249
NM_000153.4(GALC):c.1671-15C>T	rs12432149	0.45011
NM_000153.4(GALC):c.1350C>T (p.Ser450=)	rs398076	0.39608
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.742G>A (p.Asp248Asn)	rs34362748	0.11424
NM_000153.4(GALC):c.621+24T>C	rs45568734	0.11420
NM_000153.4(GALC):c.329-35G>A	rs77466023	0.11380
NM_000153.4(GALC):c.1161+38T>C	rs17687109	0.11289
NM_000153.4(GALC):c.75C>A (p.Gly25=)	rs111976362	0.11287
NM_000153.4(GALC):c.42G>C (p.Ala14=)	rs112992946	0.11183
NM_000153.4(GALC):c.61G>C (p.Ala21Pro)	rs111887056	0.11180
NM_000153.4(GALC):c.550C>T (p.Arg184Cys)	rs1805078	0.03875
NM_000153.4(GALC):c.330C>T (p.Asp110=)	rs11552556	0.03162
NM_000153.4(GALC):c.397T>C (p.Leu133=)	rs56194647	0.02392
NM_000153.4(GALC):c.1072C>T (p.Leu358=)	rs74073730	0.01792
NM_000153.4(GALC):c.1302C>T (p.Ser434=)	rs3213918	0.00674
NM_000153.4(GALC):c.1403C>G (p.Thr468Ser)	rs34134328	0.00449
NM_000153.4(GALC):c.96G>T (p.Leu32=)	rs113719127	0.00324
NM_000153.4(GALC):c.913A>G (p.Ile305Val)	rs74887188	0.00270
NM_000153.4(GALC):c.956A>G (p.Tyr319Cys)	rs183105855	0.00044
NM_000153.4(GALC):c.1731C>T (p.Phe577=)	rs201560122	0.00006
NM_000153.3(GALC):c.1834+22dup	rs34752717
NM_000153.4(GALC):c.1162-4del	rs11300320

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