ClinVar Miner

List of variants in gene LOC130064074, NDUFA13 studied for thyroid gland disorder

Included ClinVar conditions (105):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 3
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HGVS dbSNP gnomAD frequency
NM_015965.7(NDUFA13):c.15G>C (p.Lys5Asn) rs137852869
NM_015965.7(NDUFA13):c.44dup (p.Tyr16fs)
NM_015965.7(NDUFA13):c.94+1G>A

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