Variants in gene DYSF with conflicting interpretations "pathogenic" and "uncertain significance"

Submission 1 (pathogenic) minimum review status:		Submission 1 (pathogenic) method:
Submission 2 (uncertain significance) minimum review status:		Submission 2 (uncertain significance) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 10

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HGVS	dbSNP	gnomAD frequency
NM_001130987.2(DYSF):c.4859G>A (p.Arg1620His)	rs185596534	0.00072
NM_001130987.2(DYSF):c.3175C>T (p.Arg1059Cys)	rs144598063	0.00014
NM_001130987.2(DYSF):c.4078C>T (p.Arg1360Trp)	rs199870606	0.00010
NM_001130987.2(DYSF):c.5420G>A (p.Arg1807Gln)	rs148860301	0.00003
NM_001130987.2(DYSF):c.1609G>A (p.Gly537Arg)	rs121908962	0.00001
NM_001130987.2(DYSF):c.1906G>A (p.Gly636Arg)	rs201049092	0.00001
NM_001130987.2(DYSF):c.3167G>A (p.Arg1056Gln)	rs150877497	0.00001
NM_001130987.2(DYSF):c.5557C>T (p.Arg1853Cys)	rs1280185461	0.00001
NM_001130987.2(DYSF):c.410del (p.Pro137fs)	rs886043342
NM_001130987.2(DYSF):c.5150G>C (p.Cys1717Ser)	rs753279446

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