List of variants in gene CSRP3 reported as uncertain significance by Joint Genome Diagnostic Labs from Nijmegen and Maastricht, Radboudumc and MUMC+

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: 7

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HGVS	dbSNP	gnomAD frequency
NM_003476.5(CSRP3):c.379G>A (p.Val127Ile)	rs149201422	0.00009
NM_003476.5(CSRP3):c.535A>G (p.Thr179Ala)	rs397516859	0.00005
NM_003476.5(CSRP3):c.365G>A (p.Arg122Gln)	rs193922667	0.00004
NM_003476.5(CSRP3):c.140C>T (p.Thr47Met)	rs397516851	0.00003
NM_003476.5(CSRP3):c.437G>A (p.Arg146His)	rs377066670	0.00002
NM_003476.5(CSRP3):c.208G>T (p.Gly70Trp)	rs777211110
NM_003476.5(CSRP3):c.265G>T (p.Gly89Cys)	rs367827746

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