List of variants in gene DYSF reported as likely benign by Counsyl

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: 15

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HGVS	dbSNP	gnomAD frequency
NM_001130987.2(DYSF):c.1216G>C (p.Val406Leu)	rs150724610	0.00580
NM_001130987.2(DYSF):c.386G>A (p.Gly129Glu)	rs34997054	0.00411
NM_001130987.2(DYSF):c.3779G>A (p.Arg1260His)	rs2303603	0.00049
NM_001130987.2(DYSF):c.3114G>A (p.Pro1038=)	rs398123778	0.00005
NM_001130987.2(DYSF):c.2016C>T (p.Asn672=)	rs199565036	0.00004
NM_001130987.2(DYSF):c.5841C>T (p.Phe1947=)	rs772521748	0.00002
NM_001130987.2(DYSF):c.2706C>T (p.Asn902=)	rs398123775	0.00001
NM_001130987.2(DYSF):c.3477G>A (p.Thr1159=)	rs576460368	0.00001
NM_001130987.2(DYSF):c.1149+7A>T	rs771741504
NM_001130987.2(DYSF):c.3086-17G>T	rs3764971
NM_001130987.2(DYSF):c.3228+8_3228+33del	rs1553556251
NM_001130987.2(DYSF):c.4478_4481dup (p.Ser1495fs)	rs1553389065
NM_001130987.2(DYSF):c.4494dup (p.Thr1499fs)	rs1553389118
NM_001130987.2(DYSF):c.46AAG[1] (p.Lys17del)	rs1553501109
NM_003494.4(DYSF):c.75C>T (p.Ser25=)	rs375772222

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