Variants in gene GALNS 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: 12

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HGVS	dbSNP	gnomAD frequency
NM_000512.5(GALNS):c.199C>A (p.Leu67Met)	rs11862754	0.10099
NM_000512.5(GALNS):c.240G>A (p.Ser80=)	rs11865929	0.01724
NM_000512.5(GALNS):c.1002+17C>T	rs78494153	0.01020
NM_000512.5(GALNS):c.*3C>G	rs77826920	0.01005
NM_000512.5(GALNS):c.121-210C>T	rs75552025	0.00974
NM_000512.5(GALNS):c.723C>T (p.Ala241=)	rs117053987	0.00855
NM_000512.5(GALNS):c.775C>A (p.Arg259=)	rs61742258	0.00707
NM_000512.5(GALNS):c.1003-42C>T	rs139088253	0.00674
NM_000512.5(GALNS):c.359C>T (p.Ser120Leu)	rs112454391	0.00404
NM_000512.5(GALNS):c.303C>T (p.Asn101=)	rs79146426	0.00092
NM_000512.5(GALNS):c.633+22T>C	rs201579340	0.00045
NM_000512.5(GALNS):c.567-3C>T	rs549597016	0.00001

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