ClinVar Miner

Submissions for variant NM_080669.6(SLC46A1):c.439G>C (p.Gly147Arg)

dbSNP: rs80338771
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
GeneReviews RCV000020950 SCV000041574 not provided Congenital defect of folate absorption no assertion provided literature only
UniProtKB/Swiss-Prot RCV000059715 SCV000091285 not provided not provided no assertion provided not provided

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