ClinVar Miner

List of variants in gene ANKH reported as likely benign for arthritis

Included ClinVar conditions (10):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 8
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HGVS dbSNP
NM_054027.6(ANKH):c.-291_-289CCG[8] rs531421951
NM_054027.6(ANKH):c.1012-11T>G rs576472902
NM_054027.6(ANKH):c.102G>A (p.Leu34=) rs116591972
NM_054027.6(ANKH):c.258C>T (p.Ala86=) rs74355706
NM_054027.6(ANKH):c.405C>T (p.Leu135=) rs149656955
NM_054027.6(ANKH):c.432+13G>A rs112742497
NM_054027.6(ANKH):c.560G>A (p.Arg187Gln) rs146886108
NM_054027.6(ANKH):c.681G>A (p.Glu227=) rs144687394

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