List of variants in gene combination ALG12, ZBED4 reported as likely benign

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: 12

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HGVS	dbSNP	gnomAD frequency
NM_014838.3(ZBED4):c.586G>A (p.Ala196Thr)	rs199553823	0.00006
NM_014838.3(ZBED4):c.736G>A (p.Gly246Ser)	rs371904225	0.00006
NM_014838.3(ZBED4):c.2803C>T (p.Arg935Cys)	rs1056271900	0.00001
NM_014838.3(ZBED4):c.3407A>G (p.Asn1136Ser)	rs769042463	0.00001
NM_014838.3(ZBED4):c.37G>A (p.Gly13Ser)	rs753308540	0.00001
NM_014838.3(ZBED4):c.1435T>C (p.Tyr479His)
NM_014838.3(ZBED4):c.2672A>G (p.Lys891Arg)
NM_014838.3(ZBED4):c.2725A>G (p.Ile909Val)
NM_014838.3(ZBED4):c.3325G>T (p.Ala1109Ser)
NM_014838.3(ZBED4):c.3346G>A (p.Ala1116Thr)
NM_014838.3(ZBED4):c.715A>G (p.Met239Val)
NM_014838.3(ZBED4):c.821G>A (p.Ser274Asn)

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