List of variants in gene ARHGEF9 reported as likely pathogenic 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: 6

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HGVS	dbSNP	gnomAD frequency
NM_001353921.2(ARHGEF9):c.1088G>A (p.Arg363Gln)	rs1556335112	0.00001
NM_001353921.2(ARHGEF9):c.1033C>T (p.Arg345Trp)	rs869312941
NM_001353921.2(ARHGEF9):c.1034G>A (p.Arg345Gln)	rs2147265791
NM_001353921.2(ARHGEF9):c.1115G>A (p.Arg372His)	rs2048831313
NM_001353921.2(ARHGEF9):c.1261dup (p.Ile421fs)	rs1602253507
NM_001353921.2(ARHGEF9):c.1322-1G>A

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