List of variants in gene WDR62 reported as 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: 3

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HGVS	dbSNP	gnomAD frequency
GRCh37/hg19 19q13.12(chr19:36572335-36574143)x3
NM_001083961.2(WDR62):c.2864_2867del (p.Asp955fs)	rs757827840
NM_001083961.2(WDR62):c.600_601del (p.Arg200fs)

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