ClinVar Miner

Submissions for variant NM_020754.4(ARHGAP31):c.1533A>G (p.Thr511=)

gnomAD frequency: 0.02008  dbSNP: rs77678258
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
Invitae RCV000893279 SCV001037201 benign not provided 2024-01-22 criteria provided, single submitter clinical testing
GeneDx RCV000893279 SCV001865269 benign not provided 2018-11-08 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV002259914 SCV002539428 benign Adams-Oliver syndrome 1 2021-12-05 criteria provided, single submitter clinical testing

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