List of variants in gene SPRED1 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
NM_152594.3(SPRED1):c.70C>T (p.Arg24Ter)	rs121434313	0.00001
GRCh37/hg19 15q14(chr15:38556565-38591748)x1
NM_152594.3(SPRED1):c.1149_1152del (p.Gly385fs)	rs1595763925

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