ClinVar Miner

List of variants in gene HECW2 reported as likely pathogenic by CeGaT Center for Human Genetics Tuebingen

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: 2

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HGVS	dbSNP	gnomAD frequency
NM_001348768.2(HECW2):c.3571C>T (p.Arg1191Trp)	rs1575279293
NM_001348768.2(HECW2):c.4355G>C (p.Gly1452Ala)

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