List of variants in gene PRKCD reported as likely pathogenic for autoimmune disease

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_006254.4(PRKCD):c.788-2A>G	rs1295207359	0.00001
NM_006254.4(PRKCD):c.1073G>A (p.Gly358Asp)
NM_006254.4(PRKCD):c.1743+2T>A	rs2471106746
NM_006254.4(PRKCD):c.571+1G>A	rs1703450134
NM_006254.4(PRKCD):c.657+1G>A
NM_006254.4(PRKCD):c.788-1G>T	rs2471094850

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