List of variants in gene PSG1 reported as likely benign for not specified

Minimum submission review status:		Collection method:
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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 9

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HGVS	dbSNP	gnomAD frequency
NM_001184825.2(PSG1):c.1234G>A (p.Glu412Lys)	rs138243478	0.00052
NM_001184825.2(PSG1):c.925C>G (p.Gln309Glu)	rs748468852	0.00006
NM_001184825.2(PSG1):c.418T>G (p.Phe140Val)	rs747040462	0.00003
NM_001184825.2(PSG1):c.1187T>C (p.Val396Ala)	rs767495905	0.00002
NM_001184825.2(PSG1):c.1087C>G (p.Gln363Glu)	rs369619795
NM_001184825.2(PSG1):c.1145G>C (p.Arg382Pro)	rs150536125
NM_001184825.2(PSG1):c.410G>A (p.Arg137His)	rs1071707
NM_001184825.2(PSG1):c.576C>G (p.Ser192Arg)	rs142121865
NM_001184825.2(PSG1):c.912A>T (p.Glu304Asp)

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