List of variants in gene combination LOC129936895, PRKCD reported as likely benign for autoimmune disease

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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: 8

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HGVS	dbSNP	gnomAD frequency
NM_006254.4(PRKCD):c.372C>T (p.Asp124=)	rs148137939	0.00015
NM_006254.4(PRKCD):c.339G>A (p.Lys113=)
NM_006254.4(PRKCD):c.343T>C (p.Leu115=)
NM_006254.4(PRKCD):c.360T>C (p.Tyr120=)
NM_006254.4(PRKCD):c.376+12C>T
NM_006254.4(PRKCD):c.376+13T>G	rs781826392
NM_006254.4(PRKCD):c.376+15G>T
NM_006254.4(PRKCD):c.376+9T>C	rs2107262029

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