List of variants in gene ARHGEF1 reported as uncertain significance for Immunodeficiency 62

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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: 5

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HGVS	dbSNP	gnomAD frequency
NM_004706.4(ARHGEF1):c.2149G>A (p.Glu717Lys)	rs201127336	0.00027
NM_004706.4(ARHGEF1):c.2522C>T (p.Ala841Val)	rs375950739	0.00005
NM_004706.4(ARHGEF1):c.130A>G (p.Ser44Gly)	rs2513761262
NM_004706.4(ARHGEF1):c.205C>T (p.Gln69Ter)
NM_004706.4(ARHGEF1):c.424G>A (p.Val142Met)	rs2513786999

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