List of variants in gene PXDN reported as likely benign by CeGaT Center for Human Genetics Tuebingen

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: 6

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HGVS	dbSNP	gnomAD frequency
NM_012293.3(PXDN):c.1113G>A (p.Pro371=)	rs200996147	0.00399
NM_012293.3(PXDN):c.1176G>T (p.Thr392=)	rs140056124	0.00223
NM_012293.3(PXDN):c.1656C>T (p.Pro552=)	rs200276592	0.00066
NM_012293.3(PXDN):c.474G>A (p.Pro158=)	rs371424352	0.00004
NM_012293.3(PXDN):c.2586C>T (p.Ile862=)
NM_012293.3(PXDN):c.780G>A (p.Gly260=)

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