ClinVar Miner

List of variants in gene LOXHD1 reported as likely benign by Illumina Clinical Services Laboratory,Illumina

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 6
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HGVS dbSNP
NM_144612.6(LOXHD1):c.2175C>T (p.Asn725=) rs2086005
NM_144612.6(LOXHD1):c.2473G>A (p.Val825Met) rs36086089
NM_144612.6(LOXHD1):c.3463A>G (p.Arg1155Gly) rs1893566
NM_144612.6(LOXHD1):c.5213+13G>A rs59128481
NM_144612.6(LOXHD1):c.5997-11del rs143514947
NM_144612.6(LOXHD1):c.6107C>T (p.Ala2036Val) rs1377016

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