List of variants in gene ALG12 reported as benign for congenital disorder of glycosylation type I

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 32

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HGVS	dbSNP	gnomAD frequency
NM_024105.4(ALG12):c.885A>G (p.Ala295=)	rs8135963	0.36465
NM_024105.4(ALG12):c.*51A>G	rs1321	0.25423
NM_024105.4(ALG12):c.664+9G>C	rs9616368	0.23841
NM_024105.4(ALG12):c.664+12A>G	rs9616204	0.23839
NM_024105.4(ALG12):c.-141T>C	rs9616378	0.22442
NM_024105.4(ALG12):c.1177A>G (p.Ile393Val)	rs3922872	0.09076
NM_024105.4(ALG12):c.163-19C>A	rs11705497	0.07946
NM_024105.4(ALG12):c.99G>A (p.Val33=)	rs76707654	0.04368
NM_024105.4(ALG12):c.*240G>A	rs76848348	0.03225
NM_024105.4(ALG12):c.1029G>A (p.Ala343=)	rs62233155	0.02811
NM_024105.4(ALG12):c.*280G>A	rs116765369	0.02266
NM_024105.4(ALG12):c.469+13C>T	rs78916708	0.01349
NM_024105.4(ALG12):c.939C>T (p.Ile313=)	rs114335781	0.00874
NM_024105.4(ALG12):c.768+17G>A	rs145358718	0.00827
NM_024105.4(ALG12):c.645G>A (p.Pro215=)	rs12167668	0.00577
NM_024105.4(ALG12):c.698G>A (p.Arg233Gln)	rs114264124	0.00516
NM_024105.4(ALG12):c.631C>T (p.Arg211Cys)	rs144665682	0.00490
NM_024105.4(ALG12):c.1163-19G>A	rs200745798	0.00396
NM_024105.4(ALG12):c.48G>C (p.Leu16=)	rs143508665	0.00377
NM_024105.4(ALG12):c.1155C>T (p.Pro385=)	rs113652023	0.00282
NM_024105.4(ALG12):c.501C>T (p.His167=)	rs149845730	0.00212
NM_024105.4(ALG12):c.359G>A (p.Arg120Gln)	rs117687848	0.00169
NM_024105.4(ALG12):c.768+16C>T	rs558809803	0.00083
NM_024105.4(ALG12):c.1362C>T (p.Val454=)	rs12163163	0.00041
NM_024105.4(ALG12):c.465T>C (p.Pro155=)	rs201564211	0.00037
NM_024105.4(ALG12):c.189C>T (p.Val63=)	rs190345740	0.00011
NM_024105.4(ALG12):c.469+14G>A	rs76905919	0.00006
NM_024105.4(ALG12):c.639C>T (p.Ala213=)	rs140835842	0.00006
NM_024105.4(ALG12):c.993-19G>A	rs185216992	0.00004
NM_024105.4(ALG12):c.1047C>G (p.Ile349Met)	rs182006999
NM_024105.4(ALG12):c.162+12del
NM_024105.4(ALG12):c.406A>G (p.Met136Val)

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