List of variants in gene GALNS reported as benign by Mayo Clinic Laboratories, Mayo Clinic

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: 18

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HGVS	dbSNP	gnomAD frequency
NM_000512.5(GALNS):c.708C>T (p.His236=)	rs1064315	0.24874
NM_000512.5(GALNS):c.634-19G>A	rs12934499	0.20916
NM_000512.5(GALNS):c.244+19C>T	rs35137494	0.13406
NM_000512.5(GALNS):c.199C>A (p.Leu67Met)	rs11862754	0.10099
NM_000512.5(GALNS):c.634-20C>T	rs17603837	0.08794
NM_000512.5(GALNS):c.1177G>T (p.Ala393Ser)	rs2303269	0.05170
NM_000512.5(GALNS):c.758+22C>T	rs78317153	0.04917
NM_000512.5(GALNS):c.898+25C>G	rs113936280	0.04554
NM_000512.5(GALNS):c.599C>T (p.Thr200Met)	rs7187889	0.04495
NM_000512.5(GALNS):c.692C>G (p.Ala231Gly)	rs34745339	0.04350
NM_000512.5(GALNS):c.846C>T (p.Phe282=)	rs35232749	0.03726
NM_000512.5(GALNS):c.510T>C (p.Tyr170=)	rs3743544	0.03694
NM_000512.5(GALNS):c.318C>T (p.Asn106=)	rs34278797	0.01971
NM_000512.5(GALNS):c.566+10C>T	rs77514811	0.01544
NM_000512.5(GALNS):c.1278G>T (p.Gly426=)	rs76651187	0.01075
NM_000512.5(GALNS):c.*3C>G	rs77826920	0.01005
NM_000512.5(GALNS):c.566+30C>T	rs200659210	0.00141
NM_000512.5(GALNS):c.633+22T>C	rs201579340	0.00045

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