List of variants in gene MRPS22 reported as likely benign by CeGaT Center for Human Genetics Tuebingen

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_020191.4(MRPS22):c.741C>G (p.His247Gln)	rs140631494	0.00357
NM_020191.4(MRPS22):c.938C>T (p.Ser313Leu)	rs147932653	0.00066
NM_020191.4(MRPS22):c.321T>C (p.Thr107=)	rs150391961	0.00004
NM_020191.4(MRPS22):c.519C>T (p.Val173=)

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