ClinVar Miner

List of variants in gene combination LOC101927178, PPP2R3C reported by School of Medicine, Marmara University

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_017917.4(PPP2R3C):c.578T>C (p.Leu193Ser)	rs1566411552	0.00001
NM_017917.4(PPP2R3C):c.1049T>C (p.Phe350Ser)	rs1566684983
NM_017917.4(PPP2R3C):c.308T>C (p.Leu103Pro)	rs754106837

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