List of variants in gene combination PI4KA, SERPIND1 reported as uncertain significance by CeGaT Center for Human Genetics Tuebingen

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_000185.4(SERPIND1):c.842T>C (p.Ile281Thr)	rs145370736	0.00160
NM_000185.4(SERPIND1):c.749T>C (p.Ile250Thr)	rs139434064	0.00009
NM_000185.4(SERPIND1):c.1164-6G>T
NM_000185.4(SERPIND1):c.1403G>A (p.Arg468His)
NM_000185.4(SERPIND1):c.941G>A (p.Arg314Gln)	rs142500721
NM_000185.4(SERPIND1):c.973A>G (p.Met325Val)

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