List of variants in gene combination MAF, WWOX reported as benign for electroclinical syndrome

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: 7

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HGVS	dbSNP	gnomAD frequency
NM_016373.4(WWOX):c.1238C>A (p.Ser413Tyr)	rs117065412	0.01316
NM_016373.4(WWOX):c.1134C>T (p.Asn378=)	rs201088847	0.00274
NM_016373.4(WWOX):c.1197G>A (p.Ala399=)	rs376935572	0.00203
NM_016373.4(WWOX):c.1141C>T (p.Arg381Cys)	rs200461412	0.00083
NM_016373.4(WWOX):c.1228G>T (p.Gly410Cys)	rs76204496	0.00009
NM_016373.4(WWOX):c.1057-14T>C	rs66481974
NM_016373.4(WWOX):c.1239C>T (p.Ser413=)	rs199576434

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