List of variants in gene MOCS2 reported as uncertain significance 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: 9

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HGVS	dbSNP	gnomAD frequency
NM_004531.5(MOCS2):c.108G>A (p.Met36Ile)	rs140563222	0.00064
NM_004531.5(MOCS2):c.296C>T (p.Ala99Val)	rs2233217	0.00049
NM_176806.4(MOCS2):c.146C>G (p.Ala49Gly)	rs766341488	0.00011
NM_004531.5(MOCS2):c.415G>A (p.Val139Met)	rs199581021	0.00004
NM_004531.5(MOCS2):c.74A>G (p.Glu25Gly)	rs749876758	0.00002
NM_004531.5(MOCS2):c.57A>T (p.Leu19Phe)	rs776441627	0.00001
NM_176806.4(MOCS2):c.61G>T (p.Val21Phe)	rs759021832	0.00001
NM_004531.5(MOCS2):c.244T>G (p.Phe82Val)	rs1579932680
NM_176806.4(MOCS2):c.79T>C (p.Ser27Pro)	rs1579937471

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