ClinVar Miner

Submissions for variant NM_001854.4(COL11A1):c.3231G>A (p.Pro1077=)

gnomAD frequency: 0.00096  dbSNP: rs147247206
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Eurofins Ntd Llc (ga) RCV000733673 SCV000861766 uncertain significance not provided 2018-06-25 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000733673 SCV001102463 benign not provided 2024-01-13 criteria provided, single submitter clinical testing
GeneDx RCV000733673 SCV001823292 likely benign not provided 2021-09-07 criteria provided, single submitter clinical testing

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