ClinVar Miner

List of variants in gene LOXHD1 reported as likely benign for not provided

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Total variants: 21
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HGVS dbSNP
NM_144612.6(LOXHD1):c.1313A>G (p.Lys438Arg) rs186138859
NM_144612.6(LOXHD1):c.1570C>T (p.Arg524Cys) rs192376005
NM_144612.6(LOXHD1):c.1945G>A (p.Asp649Asn) rs141932807
NM_144612.6(LOXHD1):c.2027A>G (p.Asp676Gly) rs16978578
NM_144612.6(LOXHD1):c.2080G>T (p.Asp694Tyr) rs35727744
NM_144612.6(LOXHD1):c.2871G>A (p.Ser957=) rs181591912
NM_144612.6(LOXHD1):c.2916_2924AGAGGAGGA[1] (p.Glu976_Glu978del) rs765944082
NM_144612.6(LOXHD1):c.3350+92G>A
NM_144612.6(LOXHD1):c.3619+9G>A
NM_144612.6(LOXHD1):c.457C>T (p.Arg153Cys) rs112618498
NM_144612.6(LOXHD1):c.4584G>A (p.Lys1528=)
NM_144612.6(LOXHD1):c.4635G>A (p.Val1545=)
NM_144612.6(LOXHD1):c.4860C>T (p.Tyr1620=)
NM_144612.6(LOXHD1):c.4962G>A (p.Glu1654=)
NM_144612.6(LOXHD1):c.5023C>T (p.Arg1675Cys) rs201060702
NM_144612.6(LOXHD1):c.5085+74G>A
NM_144612.6(LOXHD1):c.5213+6T>C
NM_144612.6(LOXHD1):c.6066C>T (p.His2022=) rs753440039
NM_144612.6(LOXHD1):c.6147C>T (p.Tyr2049=) rs374858340
NM_144612.6(LOXHD1):c.883+56C>T
NM_144612.6:c.4531-19C>T

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