List of variants in gene PARN reported as likely benign by Genetic Services Laboratory, University of Chicago

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: 13

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HGVS	dbSNP	gnomAD frequency
NM_002582.4(PARN):c.1761C>T (p.Ser587=)	rs148052946	0.00110
NM_002582.4(PARN):c.1782C>T (p.Thr594=)	rs187555579	0.00107
NM_002582.4(PARN):c.1263-8T>G	rs182460499	0.00097
NM_002582.4(PARN):c.825C>T (p.His275=)	rs374114285	0.00073
NM_002582.4(PARN):c.1102A>T (p.Ser368Cys)	rs138984302	0.00050
NM_002582.4(PARN):c.1464C>T (p.Pro488=)	rs61748886	0.00050
NM_002582.4(PARN):c.1406-9C>T	rs530099133	0.00019
NM_002582.4(PARN):c.389-8G>A	rs200322751	0.00019
NM_002582.4(PARN):c.978A>G (p.Lys326=)	rs200678657	0.00017
NM_002582.4(PARN):c.702+5C>T	rs368739970	0.00009
NM_002582.4(PARN):c.327+10A>G	rs773687682	0.00004
NM_002582.4(PARN):c.540T>C (p.Phe180=)	rs375818973	0.00003
NM_002582.4(PARN):c.453A>T (p.Ser151=)	rs911902351	0.00002

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