List of variants in gene PORCN reported as likely benign for Inborn genetic diseases

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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_203475.3(PORCN):c.1274C>T (p.Thr425Ile)	rs146322406	0.00044
NM_203475.3(PORCN):c.794C>T (p.Thr265Met)	rs200707168	0.00009
NM_203475.3(PORCN):c.683G>A (p.Arg228His)	rs373691543	0.00005
NM_203475.3(PORCN):c.112G>A (p.Ala38Thr)	rs782505896	0.00003
NM_203475.3(PORCN):c.325A>G (p.Met109Val)	rs781857161	0.00002
NM_203475.3(PORCN):c.9C>T (p.Thr3=)	rs1556973494	0.00002
NM_203475.3(PORCN):c.24A>G (p.Glu8=)	rs187875315	0.00001
NM_203475.3(PORCN):c.705-3T>G	rs782321472	0.00001
NM_203475.3(PORCN):c.968G>A (p.Arg323His)

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