ClinVar Miner

List of variants in gene TXNDC15 reported as likely pathogenic for Meckel syndrome, type 1

Included ClinVar conditions (6):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 2
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HGVS dbSNP
NM_024715.3(TXNDC15):c.103+1G>A rs886039792
NM_024715.3(TXNDC15):c.673_687del (p.Ser225_His229del) rs886039791

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