List of variants in gene ARPC1B reported as uncertain significance for Platelet abnormalities with eosinophilia and immune-mediated inflammatory 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: 9

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HGVS	dbSNP	gnomAD frequency
NM_005720.4(ARPC1B):c.1091C>T (p.Ser364Leu)	rs144187782	0.00211
NM_005720.4(ARPC1B):c.932C>G (p.Ser311Cys)	rs200946215	0.00015
NM_005720.4(ARPC1B):c.985G>A (p.Val329Ile)	rs1465318842	0.00002
NM_005720.4(ARPC1B):c.308G>A (p.Arg103His)	rs11556758	0.00001
NM_005720.4(ARPC1B):c.484T>G (p.Cys162Gly)	rs370537333	0.00001
NM_005720.4(ARPC1B):c.713C>T (p.Ala238Val)	rs369966813	0.00001
NM_005720.4(ARPC1B):c.115G>A (p.Gly39Ser)	rs148509279
NM_005720.4(ARPC1B):c.180G>A (p.Trp60Ter)
NM_005720.4(ARPC1B):c.782C>T (p.Ala261Val)

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