ClinVar Miner

List of variants in gene LOXHD1 reported as benign for not specified

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Gene type:
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Total variants: 60
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HGVS dbSNP
NM_144612.6(LOXHD1):c.1028G>A (p.Arg343His) rs183531840
NM_144612.6(LOXHD1):c.1053G>A (p.Leu351=) rs140842472
NM_144612.6(LOXHD1):c.1087G>A (p.Val363Ile) rs10163657
NM_144612.6(LOXHD1):c.1313A>G (p.Lys438Arg) rs186138859
NM_144612.6(LOXHD1):c.1431+10G>T rs57330753
NM_144612.6(LOXHD1):c.1570C>T (p.Arg524Cys) rs192376005
NM_144612.6(LOXHD1):c.1617G>A (p.Met539Ile) rs143142227
NM_144612.6(LOXHD1):c.1708G>A (p.Asp570Asn) rs140437150
NM_144612.6(LOXHD1):c.1742T>C (p.Val581Ala) rs35007621
NM_144612.6(LOXHD1):c.1752G>A (p.Thr584=) rs558087385
NM_144612.6(LOXHD1):c.177G>A (p.Thr59=) rs116413527
NM_144612.6(LOXHD1):c.1815C>T (p.Asp605=) rs201388780
NM_144612.6(LOXHD1):c.1843C>A (p.Arg615=) rs112463030
NM_144612.6(LOXHD1):c.1876G>T (p.Gly626Cys) rs34589386
NM_144612.6(LOXHD1):c.1894G>T (p.Gly632Cys) rs35088381
NM_144612.6(LOXHD1):c.1944C>T (p.Ser648=) rs369039902
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.2175C>T (p.Asn725=) rs2086005
NM_144612.6(LOXHD1):c.2264G>T (p.Gly755Val) rs188517529
NM_144612.6(LOXHD1):c.2307C>T (p.Ser769=) rs115658952
NM_144612.6(LOXHD1):c.2370C>T (p.Asp790=) rs34723936
NM_144612.6(LOXHD1):c.2473G>A (p.Val825Met) rs36086089
NM_144612.6(LOXHD1):c.2599-11C>T rs150139569
NM_144612.6(LOXHD1):c.274G>A (p.Val92Ile) rs115275492
NM_144612.6(LOXHD1):c.2816_2818AGA[3] (p.Lys942del) rs142960762
NM_144612.6(LOXHD1):c.2871G>A (p.Ser957=) rs181591912
NM_144612.6(LOXHD1):c.2T>A (p.Met1Lys) rs36024592
NM_144612.6(LOXHD1):c.3090G>A (p.Thr1030=) rs113994614
NM_144612.6(LOXHD1):c.3269G>A (p.Arg1090Gln) rs118174674
NM_144612.6(LOXHD1):c.3463A>G (p.Arg1155Gly) rs1893566
NM_144612.6(LOXHD1):c.3619+9G>A
NM_144612.6(LOXHD1):c.3999C>T (p.Cys1333=) rs117297079
NM_144612.6(LOXHD1):c.4031G>T (p.Cys1344Phe) rs368870055
NM_144612.6(LOXHD1):c.4148C>G (p.Thr1383Arg) rs7244681
NM_144612.6(LOXHD1):c.4148C>T (p.Thr1383Met) rs7244681
NM_144612.6(LOXHD1):c.4217C>T (p.Ala1406Val) rs146739496
NM_144612.6(LOXHD1):c.4440G>A (p.Val1480=) rs76946640
NM_144612.6(LOXHD1):c.4526G>A (p.Gly1509Glu) rs187587197
NM_144612.6(LOXHD1):c.4531-19C>T rs117403100
NM_144612.6(LOXHD1):c.457C>T (p.Arg153Cys) rs112618498
NM_144612.6(LOXHD1):c.4714C>A (p.Arg1572=) rs75949023
NM_144612.6(LOXHD1):c.4868A>G (p.Glu1623Gly) rs12606417
NM_144612.6(LOXHD1):c.5213+13G>A rs59128481
NM_144612.6(LOXHD1):c.5214-3C>T rs528236655
NM_144612.6(LOXHD1):c.5503C>T (p.Leu1835=) rs202043044
NM_144612.6(LOXHD1):c.5506+12G>A rs200518261
NM_144612.6(LOXHD1):c.5667G>A (p.Lys1889=) rs201366522
NM_144612.6(LOXHD1):c.5682C>T (p.His1894=) rs114974101
NM_144612.6(LOXHD1):c.5848G>A (p.Glu1950Lys) rs79045813
NM_144612.6(LOXHD1):c.5913C>T (p.Asn1971=) rs146200756
NM_144612.6(LOXHD1):c.5997-11del rs143514947
NM_144612.6(LOXHD1):c.6084G>A (p.Arg2028=) rs367833904
NM_144612.6(LOXHD1):c.6107C>T (p.Ala2036Val) rs1377016
NM_144612.6(LOXHD1):c.611-15T>C rs146912450
NM_144612.6(LOXHD1):c.6398G>A (p.Arg2133His) rs74316327
NM_144612.6(LOXHD1):c.6413G>A (p.Arg2138Gln) rs148468627
NM_144612.6(LOXHD1):c.6555C>T (p.Ala2185=) rs189873733
NM_144612.6(LOXHD1):c.6597G>A (p.Gly2199=) rs115835484
NM_144612.6(LOXHD1):c.966G>C (p.Gly322=) rs114082868

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