ClinVar Miner

List of variants in gene SLC39A13 reported as benign for Ehlers-Danlos syndrome

Included ClinVar conditions (34):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 3
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HGVS dbSNP
NM_152264.4(SLC39A13):c.1053G>A (p.Ala351=) rs576702857
NM_152264.4(SLC39A13):c.119G>A (p.Arg40Gln) rs35741412
NM_152264.4(SLC39A13):c.83G>A (p.Gly28Glu) rs2010519

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