List of variants in gene DYSF reported as likely benign by Athena Diagnostics Inc

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: 25

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HGVS	dbSNP	gnomAD frequency
NM_001130987.2(DYSF):c.3337C>T (p.Arg1113Cys)	rs141536854	0.00601
NM_001130987.2(DYSF):c.2642A>C (p.Asp881Ala)	rs35884879	0.00589
NM_001130987.2(DYSF):c.4027A>G (p.Ile1343Val)	rs145401010	0.00428
NM_001130987.2(DYSF):c.1288G>A (p.Val430Met)	rs144202114	0.00373
NM_001130987.2(DYSF):c.1145C>T (p.Ala382Val)	rs115279465	0.00342
NM_001130987.2(DYSF):c.3968C>A (p.Thr1323Lys)	rs116426399	0.00200
NM_001130987.2(DYSF):c.5503C>T (p.Arg1835Trp)	rs139879284	0.00161
NM_001130987.2(DYSF):c.4756-3C>T	rs371227553	0.00153
NM_001130987.2(DYSF):c.4937T>C (p.Ile1646Thr)	rs146384562	0.00124
NM_001130987.2(DYSF):c.4629C>G (p.Val1543=)	rs142483266	0.00109
NM_001130987.2(DYSF):c.1447A>G (p.Met483Val)	rs141818764	0.00096
NM_001130987.2(DYSF):c.6174-9C>T	rs201070766	0.00075
NM_001130987.2(DYSF):c.4993G>A (p.Val1665Ile)	rs147056383	0.00057
NM_001130987.2(DYSF):c.3779G>A (p.Arg1260His)	rs2303603	0.00049
NM_001130987.2(DYSF):c.4254C>T (p.Pro1418=)	rs142769942	0.00045
NM_001130987.2(DYSF):c.3086-9C>T	rs185350547	0.00036
NM_001130987.2(DYSF):c.1407G>A (p.Thr469=)	rs150093305	0.00026
NM_001130987.2(DYSF):c.4050C>T (p.Thr1350=)	rs138751942	0.00024
NM_001130987.2(DYSF):c.5022C>T (p.Cys1674=)	rs149989207	0.00018
NM_001130987.2(DYSF):c.3852G>A (p.Pro1284=)	rs139983909	0.00016
NM_001130987.2(DYSF):c.1140C>T (p.Asp380=)	rs373744398	0.00015
NM_001130987.2(DYSF):c.1149T>G (p.Pro383=)	rs199955501	0.00010
NM_001130987.2(DYSF):c.2820C>T (p.Ala940=)	rs373328706	0.00004
NM_001130987.2(DYSF):c.4713G>A (p.Thr1571=)	rs369750372	0.00004
NM_001130987.2(DYSF):c.5403G>A (p.Pro1801=)	rs771738959	0.00001

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