ClinVar Miner

List of variants in gene combination ANKH, LOC100130744, OTULIN reported as likely benign for chondrocalcinosis

Included ClinVar conditions (2):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 5
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HGVS dbSNP
NM_054027.6(ANKH):c.1237G>A (p.Ala413Thr) rs112513380
NM_054027.6(ANKH):c.1272C>T (p.His424=) rs201295416
NM_054027.6(ANKH):c.1278G>A (p.Ala426=) rs568804732
NM_054027.6(ANKH):c.1332C>T (p.Val444=) rs139351002
NM_054027.6(ANKH):c.1338C>T (p.Ile446=) rs756749018

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