List of variants in gene SPATA7 reported as benign by Mendelics

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_018418.5(SPATA7):c.220G>A (p.Val74Met)	rs3179969	0.39047
NM_018418.4(SPATA7):c.20_23del	rs527236050
NM_018418.5(SPATA7):c.19+102del	rs5810413

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