ClinVar Miner

Submissions for variant NM_005739.4(RASGRP1):c.676-16G>T

gnomAD frequency: 0.01169  dbSNP: rs56241040
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 RCV001512452 SCV001719876 benign not provided 2024-01-31 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002501766 SCV002812549 likely benign Immunodeficiency 64 2022-02-07 criteria provided, single submitter clinical testing

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