List of variants in gene ARHGAP31 reported as uncertain significance by Neuberg Centre For Genomic Medicine, NCGM

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_020754.4(ARHGAP31):c.1807G>A (p.Glu603Lys)	rs1489263621	0.00001
NM_020754.4(ARHGAP31):c.3247G>A (p.Glu1083Lys)	rs2107647546
NM_020754.4(ARHGAP31):c.4271del (p.Cys1424fs)	rs2472879856

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