List of variants in gene GSDME reported as benign for not specified

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: 15

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HGVS	dbSNP	gnomAD frequency
NM_001127453.2(GSDME):c.447A>G (p.Glu149=)	rs876305	0.56409
NM_001127453.2(GSDME):c.405-15G>A	rs754553	0.18061
NM_001127453.2(GSDME):c.489G>A (p.Thr163=)	rs754555	0.17320
NM_001127453.2(GSDME):c.1200A>G (p.Ala400=)	rs17149912	0.16349
NM_001127453.2(GSDME):c.619G>A (p.Val207Met)	rs12540919	0.07873
NM_001127453.2(GSDME):c.863-6T>C	rs55735863	0.03926
NM_001127453.2(GSDME):c.1199C>T (p.Ala400Val)	rs71535705	0.01715
NM_001127453.2(GSDME):c.577-15C>T	rs11970787	0.00666
NM_001127453.2(GSDME):c.658G>A (p.Gly220Ser)	rs140666247	0.00179
NM_001127453.2(GSDME):c.864G>A (p.Ala288=)	rs144358787	0.00076
NM_001127453.2(GSDME):c.1183+9A>T	rs397516910	0.00014
NM_001127453.2(GSDME):c.87T>A (p.Asp29Glu)	rs148370267	0.00010
NM_001127453.2(GSDME):c.587C>T (p.Thr196Met)	rs183361282	0.00005
NM_001127453.2(GSDME):c.1334T>A (p.Phe445Tyr)	rs61731036
NM_001127453.2(GSDME):c.424C>A (p.Pro142Thr)	rs754554

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