List of variants in gene combination LOC129936899, 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: 15

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HGVS	dbSNP	gnomAD frequency
NM_006254.4(PRKCD):c.1980C>T (p.Phe660=)	rs2230497	0.00009
NM_006254.4(PRKCD):c.1956C>T (p.Ile652=)	rs147565728	0.00006
NM_006254.4(PRKCD):c.1944C>T (p.Asp648=)	rs2471112519	0.00002
NM_006254.4(PRKCD):c.1873-19C>T	rs1483539200	0.00001
NM_006254.4(PRKCD):c.1917C>T (p.Asn639=)	rs782670259	0.00001
NM_006254.4(PRKCD):c.1941C>T (p.Ser647=)	rs781997779	0.00001
NM_006254.4(PRKCD):c.2001C>T (p.Asn667=)	rs782784858	0.00001
NM_006254.4(PRKCD):c.2010C>T (p.Phe670=)	rs781808423	0.00001
NM_006254.4(PRKCD):c.2028T>C (p.Asp676=)	rs782403404	0.00001
NM_006254.4(PRKCD):c.1873-12C>T
NM_006254.4(PRKCD):c.1873-20C>T	rs1703943861
NM_006254.4(PRKCD):c.1881C>G (p.Pro627=)	rs199634315
NM_006254.4(PRKCD):c.1881C>T (p.Pro627=)	rs199634315
NM_006254.4(PRKCD):c.1998G>A (p.Val666=)	rs1575547280
NM_006254.4(PRKCD):c.2016C>T (p.His672=)

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