List of variants in gene ARPC1B reported as likely pathogenic for not provided

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_005720.4(ARPC1B):c.311G>C (p.Trp104Ser)	rs2150894118
NM_005720.4(ARPC1B):c.393-2A>G
NM_005720.4(ARPC1B):c.989+2T>C
NM_005720.4(ARPC1B):c.990-1G>C	rs1794675671

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