ClinVar Miner

Submissions for variant NM_020754.4(ARHGAP31):c.3615C>T (p.Pro1205=)

gnomAD frequency: 0.11988  dbSNP: rs3732414
Minimum review status: Collection method:
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ClinVar version:
Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001522004 SCV001731453 benign not provided 2025-02-02 criteria provided, single submitter clinical testing
GeneDx RCV001522004 SCV001943964 benign not provided 2018-12-19 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV002259921 SCV002539441 benign Adams-Oliver syndrome 1 2021-12-05 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001522004 SCV005302948 benign not provided criteria provided, single submitter not provided

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