List of variants in gene ANXA11 studied for anterior horn disorder

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 10

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HGVS	dbSNP	gnomAD frequency
NM_145868.2(ANXA11):c.112G>A (p.Gly38Arg)	rs142083484	0.00005
NM_145868.2(ANXA11):c.1424G>A (p.Arg475Gln)	rs146644733	0.00004
NM_145868.2(ANXA11):c.119A>G (p.Asp40Gly)	rs1247392012	0.00001
NM_145868.2(ANXA11):c.1481G>A (p.Arg494Gln)	rs1318489141	0.00001
NM_145868.2(ANXA11):c.744+3G>A	rs769390362	0.00001
NM_145868.2(ANXA11):c.118G>T (p.Asp40Tyr)	rs368751524
NM_145868.2(ANXA11):c.488AGC[2] (p.Gln165del)	rs1438529241
NM_145868.2(ANXA11):c.523G>A (p.Gly175Arg)	rs754594235
NM_145868.2(ANXA11):c.607del (p.Leu203fs)
NM_145868.2(ANXA11):c.904C>T (p.Arg302Cys)	rs142183550

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