List of variants in gene GALC reported as likely benign by Illumina Clinical Services Laboratory,Illumina

Minimum submission review status:		Collection method:
Minimum conflict level:
Gene type:		Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 14

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HGVS	dbSNP
NM_000153.4(GALC):c.*1126G>A	rs1042035
NM_000153.4(GALC):c.*395C>T	rs3850376
NM_000153.4(GALC):c.*709A>C	rs45572135
NM_000153.4(GALC):c.*801A>T	rs114174103
NM_000153.4(GALC):c.1072C>T (p.Leu358=)	rs74073730
NM_000153.4(GALC):c.1302C>T (p.Ser434=)	rs3213918
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.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

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