ClinVar Miner

Submissions for variant NM_001378902.1(ROS1):c.6359G>A (p.Arg2120Gln)

gnomAD frequency: 0.00185  dbSNP: rs199882276
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000880789 SCV001023911 benign not provided 2018-07-12 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV000880789 SCV004160036 uncertain significance not provided 2023-07-01 criteria provided, single submitter clinical testing

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