List of variants in gene PLCB1 reported by Mayo Clinic Laboratories, Mayo Clinic

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: 5

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HGVS	dbSNP	gnomAD frequency
NM_015192.4(PLCB1):c.3347C>T (p.Ala1116Val)	rs148936543	0.00017
NM_015192.4(PLCB1):c.3606G>C (p.Glu1202Asp)	rs200558916	0.00007
NM_015192.4(PLCB1):c.3136G>A (p.Ala1046Thr)	rs778097231	0.00002
NM_015192.4(PLCB1):c.707G>A (p.Ser236Asn)	rs1367561790	0.00001
NM_015192.4(PLCB1):c.815A>G (p.Gln272Arg)

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