List of variants in gene combination LOC126860802, ZMYND11 reported as benign

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 12

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HGVS	dbSNP	gnomAD frequency
NM_001370100.5(ZMYND11):c.1611A>G (p.Glu537=)	rs1017361	0.94825
NM_001370100.5(ZMYND11):c.1501-15G>C	rs371996371	0.00061
NM_001370100.5(ZMYND11):c.1474C>T (p.Arg492Cys)	rs764387198	0.00004
NM_001370100.5(ZMYND11):c.1394G>A (p.Ser465Asn)	rs370171790	0.00003
NM_001370100.5(ZMYND11):c.1492C>G (p.Leu498Val)	rs750834510	0.00003
NM_001370100.5(ZMYND11):c.1282C>T (p.Pro428Ser)	rs1554793294	0.00001
NM_001370100.5(ZMYND11):c.1451C>T (p.Ser484Leu)	rs772041805	0.00001
NM_001370100.5(ZMYND11):c.1342_1344del (p.Pro448del)	rs1250648883
NM_001370100.5(ZMYND11):c.1377C>G (p.Asn459Lys)	rs774279960
NM_001370100.5(ZMYND11):c.1431C>G (p.Asp477Glu)
NM_001370100.5(ZMYND11):c.1473G>T (p.Glu491Asp)	rs1027490420
NM_001370100.5(ZMYND11):c.1553C>G (p.Ala518Gly)	rs745715509

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