List of variants in gene DYSF reported as benign by Illumina Laboratory Services, Illumina

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: 12

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HGVS	dbSNP	gnomAD frequency
NM_001130987.2(DYSF):c.1881T>C (p.Asp627=)	rs2303596	0.71202
NM_001130987.2(DYSF):c.2637A>T (p.Ser879=)	rs2288355	0.69367
NM_001130987.2(DYSF):c.1449+13C>T	rs4852801	0.60553
NM_001130987.2(DYSF):c.4062C>A (p.Ile1354=)	rs2303606	0.47852
NM_001130987.2(DYSF):c.5976A>C (p.Pro1992=)	rs17718530	0.23571
NM_001130987.2(DYSF):c.6321+15C>T	rs2559082	0.19470
NM_001130987.2(DYSF):c.4026C>T (p.Asn1342=)	rs11558179	0.18595
NM_001130987.2(DYSF):c.1276+11C>T	rs35982795	0.15096
NM_001130987.2(DYSF):c.396C>T (p.Pro132=)	rs34603128	0.14353
NM_001130987.2(DYSF):c.888+11T>C	rs13428076	0.13574
NM_003494.4(DYSF):c.-179C>A	rs6741336	0.13159
NM_001130987.2(DYSF):c.951+4T>C	rs11903960	0.09951

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