ClinVar Miner

Submissions for variant NM_003809.3(TNFSF12):c.42G>A (p.Gly14=)

gnomAD frequency: 0.00004  dbSNP: rs1170763703
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000630451 SCV000751407 likely benign Common variable immunodeficiency 2023-08-30 criteria provided, single submitter clinical testing

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