ClinVar Miner

Submissions for variant NM_000594.3(TNF):c.-1037C>T

gnomAD frequency: 0.08423  dbSNP: rs1799724
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
OMIM RCV000013196 SCV000033443 risk factor Vascular dementia, susceptibility to 2005-07-01 no assertion criteria provided literature only
OMIM RCV000013197 SCV000033444 risk factor Alzheimer disease, susceptibility to 2005-07-01 no assertion criteria provided literature only

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