List of variants in gene LIMS2 reported as benign for autosomal recessive disease

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: 16

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HGVS	dbSNP	gnomAD frequency
NM_001161403.3(LIMS2):c.399G>A (p.Lys133=)	rs4662751	0.52377
NM_001161403.3(LIMS2):c.189C>T (p.Tyr63=)	rs35765118	0.02278
NM_001161403.3(LIMS2):c.803-14C>T	rs115873946	0.02177
NM_001161403.3(LIMS2):c.803-8C>G	rs115961120	0.01430
NM_001161403.3(LIMS2):c.385C>T (p.Arg129Cys)	rs145123078	0.00587
NM_001161403.3(LIMS2):c.291G>A (p.Pro97=)	rs11900522	0.00522
NM_001161403.3(LIMS2):c.594C>T (p.Cys198=)	rs74638847	0.00282
NM_001161403.3(LIMS2):c.39C>T (p.Ala13=)	rs143117627	0.00187
NM_001161403.3(LIMS2):c.802+19T>C	rs201305372	0.00147
NM_001161403.3(LIMS2):c.661-16C>T	rs192426117	0.00121
NM_001161403.3(LIMS2):c.12-6739G>A	rs763417527	0.00034
NM_001161403.3(LIMS2):c.621C>T (p.Gly207=)	rs138162790	0.00034
NM_001161403.3(LIMS2):c.765C>T (p.Asp255=)	rs199994172	0.00014
NM_001161403.3(LIMS2):c.510-12G>A	rs374991949	0.00002
NM_001161403.3(LIMS2):c.360-4G>A	rs112254310
NM_001161403.3(LIMS2):c.441C>A (p.Ile147=)	rs199563092

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