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
NM_000153.4(GALC):c.1072C>T (p.Leu358=)	rs74073730
NM_000153.4(GALC):c.1161+38T>C	rs17687109
NM_000153.4(GALC):c.1162-4del	rs11300320
NM_000153.4(GALC):c.1302C>T (p.Ser434=)	rs3213918
NM_000153.4(GALC):c.1350C>T (p.Ser450=)	rs398076
NM_000153.4(GALC):c.1403C>G (p.Thr468Ser)	rs34134328
NM_000153.4(GALC):c.1620A>G (p.Thr540=)	rs367327
NM_000153.4(GALC):c.1671-15C>T	rs12432149
NM_000153.4(GALC):c.1685T>C (p.Ile562Thr)	rs398607
NM_000153.4(GALC):c.1698A>T (p.Val566=)	rs421466
NM_000153.4(GALC):c.1731C>T (p.Phe577=)	rs201560122
NM_000153.4(GALC):c.1834+5C>G	rs448805
NM_000153.4(GALC):c.1921A>G (p.Thr641Ala)	rs421262
NM_000153.4(GALC):c.195+19G>A	rs189853941
NM_000153.4(GALC):c.196-43C>T	rs2289511
NM_000153.4(GALC):c.328+19T>A	rs74337989
NM_000153.4(GALC):c.329-35G>A	rs77466023
NM_000153.4(GALC):c.330C>T (p.Asp110=)	rs11552556
NM_000153.4(GALC):c.397T>C (p.Leu133=)	rs56194647
NM_000153.4(GALC):c.42G>C (p.Ala14=)	rs112992946
NM_000153.4(GALC):c.550C>T (p.Arg184Cys)	rs1805078
NM_000153.4(GALC):c.61G>C (p.Ala21Pro)	rs111887056
NM_000153.4(GALC):c.621+24T>C	rs45568734
NM_000153.4(GALC):c.742G>A (p.Asp248Asn)	rs34362748
NM_000153.4(GALC):c.75C>A (p.Gly25=)	rs111976362
NM_000153.4(GALC):c.913A>G (p.Ile305Val)	rs74887188
NM_000153.4(GALC):c.956A>G (p.Tyr319Cys)	rs183105855
NM_000153.4(GALC):c.96G>T (p.Leu32=)	rs113719127
NM_000153.4(GALC):c.984G>A (p.Gln328=)	rs12888666

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