List of variants in gene ARHGEF9 reported as uncertain significance by GeneDx

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: 28

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HGVS	dbSNP	gnomAD frequency
NM_001353921.2(ARHGEF9):c.1060A>C (p.Met354Leu)	rs782248986	0.00009
NM_001353921.2(ARHGEF9):c.1175A>G (p.Asn392Ser)	rs1556334879	0.00005
NM_001353921.2(ARHGEF9):c.949G>A (p.Glu317Lys)	rs782166488	0.00003
NM_001353921.2(ARHGEF9):c.305G>A (p.Arg102Gln)	rs782087438	0.00002
NM_001353921.2(ARHGEF9):c.1018G>A (p.Gly340Ser)	rs782103101	0.00001
NM_001353921.2(ARHGEF9):c.1238T>C (p.Phe413Ser)	rs1085307842	0.00001
NM_001353921.2(ARHGEF9):c.668G>A (p.Arg223His)	rs1556365349	0.00001
NM_001353921.2(ARHGEF9):c.1034G>T (p.Arg345Leu)
NM_001353921.2(ARHGEF9):c.1126_1128dup (p.Asp376dup)	rs2048830256
NM_001353921.2(ARHGEF9):c.1276G>C (p.Ala426Pro)	rs2147217896
NM_001353921.2(ARHGEF9):c.1492G>A (p.Val498Ile)	rs2147114206
NM_001353921.2(ARHGEF9):c.1500G>T (p.Glu500Asp)	rs2147114132
NM_001353921.2(ARHGEF9):c.1540A>C (p.Asn514His)	rs1556300759
NM_001353921.2(ARHGEF9):c.1558C>T (p.Pro520Ser)	rs2147113839
NM_001353921.2(ARHGEF9):c.222C>A (p.Asn74Lys)	rs2147508871
NM_001353921.2(ARHGEF9):c.259C>A (p.Gln87Lys)	rs1602490706
NM_001353921.2(ARHGEF9):c.295T>A (p.Cys99Ser)
NM_001353921.2(ARHGEF9):c.389A>G (p.Lys130Arg)	rs1057523510
NM_001353921.2(ARHGEF9):c.430A>G (p.Arg144Gly)	rs2147450998
NM_001353921.2(ARHGEF9):c.499A>G (p.Met167Val)	rs2147450532
NM_001353921.2(ARHGEF9):c.652C>G (p.Leu218Val)	rs2050412325
NM_001353921.2(ARHGEF9):c.694C>T (p.Arg232Cys)	rs2147334395
NM_001353921.2(ARHGEF9):c.695G>A (p.Arg232His)
NM_001353921.2(ARHGEF9):c.758T>C (p.Ile253Thr)	rs2147333974
NM_001353921.2(ARHGEF9):c.820T>C (p.Tyr274His)	rs1085307467
NM_001353921.2(ARHGEF9):c.934C>A (p.Leu312Ile)	rs1057522323
NM_001353921.2(ARHGEF9):c.94C>G (p.Arg32Gly)
NM_001353921.2(ARHGEF9):c.95G>T (p.Arg32Leu)	rs782244025

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