ClinVar Miner

Submissions for variant NM_000522.5(HOXA13):c.496C>A (p.Pro166Thr)

dbSNP: rs34398255
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001679968 SCV001898743 benign not provided 2021-06-09 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001679968 SCV002363940 benign not provided 2025-01-28 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002488462 SCV002801212 benign Guttmacher syndrome; Hand-foot-genital syndrome 2022-05-03 criteria provided, single submitter clinical testing

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