List of variants in gene DCC reported as uncertain significance for amenorrhea

Minimum submission review status:		Collection method:
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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: 3

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HGVS	dbSNP	gnomAD frequency
NM_005215.4(DCC):c.1409G>A (p.Gly470Asp)	rs141813053	0.00296
NM_005215.4(DCC):c.2455G>A (p.Asp819Asn)	rs181197485	0.00033
NM_005215.4(DCC):c.2647G>A (p.Val883Ile)	rs187939463	0.00001

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