ClinVar Miner

List of variants in gene COMP reported 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
		ClinVar version:

Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_000095.3(COMP):c.1201G>T (p.Asp401Tyr)	rs2055169002
NM_000095.3(COMP):c.1405GAC[4] (p.Asp473del)	rs193922900
NM_000095.3(COMP):c.2152C>T (p.Arg718Trp)	rs28936368
NM_000095.3(COMP):c.805G>A (p.Asp269Asn)	rs2145903436

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