List of variants in gene combination GBA1, LOC106627981 reported as uncertain significance for Lewy body dementia

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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: 9

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HGVS	dbSNP	gnomAD frequency
NM_000157.4(GBA1):c.1200G>A (p.Met400Ile)	rs149487315	0.00091
NM_000157.4(GBA1):c.1224G>A (p.Thr408=)	rs138498426	0.00022
NM_000157.4(GBA1):c.1495G>A (p.Val499Met)	rs369068553	0.00006
NM_000157.4(GBA1):c.1346C>T (p.Thr449Met)	rs757930613	0.00002
NM_000157.4(GBA1):c.247C>T (p.Arg83Cys)	rs1141812	0.00002
NM_000157.4(GBA1):c.1043C>G (p.Ala348Gly)	rs78396650	0.00001
NM_000157.4(GBA1):c.1388G>C (p.Ser463Thr)	rs1571965884
NM_000157.4(GBA1):c.1506-10_1506-9delinsGA	rs1557900564
NM_000157.4(GBA1):c.454+1G>A	rs539166948

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