List of variants in gene MRPL12 reported as likely benign by GeneDx

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: 17

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HGVS	dbSNP	gnomAD frequency
NM_002949.4(MRPL12):c.480+36G>A	rs200599337	0.00579
NM_002949.4(MRPL12):c.*125G>A	rs188153315	0.00564
NM_002949.4(MRPL12):c.576C>T (p.Gly192=)	rs144790349	0.00048
NM_002949.4(MRPL12):c.261+18C>G	rs200241861	0.00037
NM_002949.4(MRPL12):c.285C>T (p.Val95=)	rs74006103	0.00035
NM_002949.4(MRPL12):c.262-33G>A	rs571761302	0.00033
NM_002949.4(MRPL12):c.-46C>T	rs373040169	0.00024
NM_002949.4(MRPL12):c.411G>A (p.Ala137=)	rs149365217	0.00023
NM_002949.4(MRPL12):c.261+5C>T	rs767787425	0.00003
NM_002949.4(MRPL12):c.528C>T (p.Val176=)	rs750264166	0.00003
NM_002949.4(MRPL12):c.261+4T>C	rs762039084	0.00001
NM_002949.4(MRPL12):c.*10C>T	rs368081864
NM_002949.4(MRPL12):c.-30A>C	rs550332320
NM_002949.4(MRPL12):c.481-13CT[3]	rs1064794897
NM_002949.4(MRPL12):c.75-120G>A	rs145265749
NM_002949.4(MRPL12):c.75-6G>A	rs534821836
NM_002949.4(MRPL12):c.87A>G (p.Pro29=)	rs576782640

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