List of variants in gene ANXA11 reported as uncertain significance for Amyotrophic lateral sclerosis type 23

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_145868.2(ANXA11):c.1424G>A (p.Arg475Gln)	rs146644733	0.00004
NM_145868.2(ANXA11):c.1010_1011delinsAA (p.Leu337Gln)	rs2132386401
NM_145868.2(ANXA11):c.607del (p.Leu203fs)
NM_145868.2(ANXA11):c.904C>T (p.Arg302Cys)	rs142183550

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