List of variants in gene ARHGAP35 reported as uncertain significance by Reproductive Endocrine Unit, Massachusetts General Hospital

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: 5

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HGVS	dbSNP	gnomAD frequency
NM_004491.5(ARHGAP35):c.4235T>C (p.Met1412Thr)	rs768641837	0.00001
NM_004491.5(ARHGAP35):c.4255C>T (p.Arg1419Cys)	rs768711914	0.00001
NM_004491.5(ARHGAP35):c.3992C>T (p.Pro1331Leu)	rs2514226692
NM_004491.5(ARHGAP35):c.4049G>A (p.Arg1350Gln)	rs757589554
NM_004491.5(ARHGAP35):c.4105C>G (p.His1369Asp)	rs1249121166

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