Variants in gene GALC with conflicting interpretations "likely benign" and "benign"

Submission 1 (likely benign) minimum review status:		Submission 1 (likely benign) method:
Submission 2 (benign) minimum review status:		Submission 2 (benign) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 14

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HGVS	dbSNP	gnomAD frequency
NM_000153.4(GALC):c.1302C>T (p.Ser434=)	rs3213918	0.00674
NM_000153.4(GALC):c.1788C>T (p.Phe596=)	rs115018138	0.00658
NM_000153.4(GALC):c.1403C>G (p.Thr468Ser)	rs34134328	0.00483
NM_000153.4(GALC):c.-66G>T	rs146439771	0.00434
NM_000153.4(GALC):c.1006G>A (p.Val336Met)	rs185073540	0.00368
NM_000153.4(GALC):c.96G>T (p.Leu32=)	rs113719127	0.00324
NM_000153.4(GALC):c.1236T>A (p.Val412=)	rs112531377	0.00321
NM_000153.4(GALC):c.-463C>T	rs181956126	0.00254
NM_000153.4(GALC):c.525C>T (p.Val175=)	rs181066089	0.00199
NM_000153.4(GALC):c.1717A>G (p.Thr573Ala)	rs200219480	0.00023
NM_000153.4(GALC):c.956A>G (p.Tyr319Cys)	rs183105855	0.00019
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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