List of variants in gene DCC reported as pathogenic by OMIM

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: 12

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HGVS	dbSNP	gnomAD frequency
NM_005215.4(DCC):c.1140+1G>A	rs797044553
NM_005215.4(DCC):c.2378T>G (p.Val793Gly)	rs1057519054
NM_005215.4(DCC):c.2414G>A (p.Gly805Glu)	rs1057519055
NM_005215.4(DCC):c.2774dup (p.Asn925fs)	rs2145024323
NM_005215.4(DCC):c.31_91+7622del
NM_005215.4(DCC):c.3836_3837del (p.Leu1279fs)	rs797044556
NM_005215.4(DCC):c.4124C>A (p.Pro1375His)	rs387906555
NM_005215.4(DCC):c.503T>C (p.Met168Thr)	rs121912967
NM_005215.4(DCC):c.571dup (p.Val191fs)	rs797044552
NM_005215.4(DCC):c.788_794del (p.Val263fs)	rs1555682265
NM_005215.4(DCC):c.823C>T (p.Arg275Ter)	rs754914260
NM_005215.4(DCC):c.925del (p.Thr309fs)	rs1057519053

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