ClinVar Miner

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

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Gene type:
ClinVar version:
Total variants: 110
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HGVS dbSNP
NC_000018.10:g.46521135C>T
NM_001173129.1(LOXHD1):c.*30G>A rs142931455
NM_144612.6(LOXHD1):c.1028G>A (p.Arg343His) rs183531840
NM_144612.6(LOXHD1):c.1071C>T (p.Pro357=) rs1391986865
NM_144612.6(LOXHD1):c.1089C>T (p.Val363=) rs578169078
NM_144612.6(LOXHD1):c.1134+11C>T rs727503149
NM_144612.6(LOXHD1):c.1134+12C>G rs1555684960
NM_144612.6(LOXHD1):c.1158T>G (p.Thr386=) rs727503148
NM_144612.6(LOXHD1):c.1162A>G (p.Ile388Val) rs115395163
NM_144612.6(LOXHD1):c.1170G>A (p.Gln390=) rs876657492
NM_144612.6(LOXHD1):c.1244T>G (p.Val415Gly) rs529972175
NM_144612.6(LOXHD1):c.1443G>A (p.Pro481=) rs184747932
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.1654+10G>A rs1200519632
NM_144612.6(LOXHD1):c.177G>A (p.Thr59=) rs116413527
NM_144612.6(LOXHD1):c.1788A>G (p.Thr596=) rs368683058
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.1887C>T (p.Ser629=) rs189550119
NM_144612.6(LOXHD1):c.1894G>A (p.Gly632Ser) rs35088381
NM_144612.6(LOXHD1):c.1945G>A (p.Asp649Asn) rs141932807
NM_144612.6(LOXHD1):c.2037G>A (p.Ala679=) rs201226222
NM_144612.6(LOXHD1):c.2100G>A (p.Thr700=) rs367826075
NM_144612.6(LOXHD1):c.2223C>T (p.Leu741=) rs199595156
NM_144612.6(LOXHD1):c.2251C>A (p.Arg751=) rs376539851
NM_144612.6(LOXHD1):c.2264G>T (p.Gly755Val) rs188517529
NM_144612.6(LOXHD1):c.2316C>T (p.Ile772=) rs876657493
NM_144612.6(LOXHD1):c.2406G>A (p.Leu802=) rs1305236679
NM_144612.6(LOXHD1):c.2448T>C (p.Tyr816=) rs1555680579
NM_144612.6(LOXHD1):c.2580G>A (p.Ala860=) rs118140267
NM_144612.6(LOXHD1):c.2664G>A (p.Gly888=) rs773487745
NM_144612.6(LOXHD1):c.2684C>G (p.Thr895Ser) rs115042043
NM_144612.6(LOXHD1):c.2841C>T (p.Asp947=) rs761010290
NM_144612.6(LOXHD1):c.2874_2891dup (p.Ser960_Ser965dup) rs759237437
NM_144612.6(LOXHD1):c.3024C>T (p.Val1008=) rs370616818
NM_144612.6(LOXHD1):c.3061+8G>T rs764128579
NM_144612.6(LOXHD1):c.3090G>A (p.Thr1030=) rs113994614
NM_144612.6(LOXHD1):c.3108C>T (p.Ala1036=) rs727503145
NM_144612.6(LOXHD1):c.3162G>A (p.Thr1054=) rs727503144
NM_144612.6(LOXHD1):c.3279C>T (p.His1093=) rs751278435
NM_144612.6(LOXHD1):c.3282C>T (p.Asp1094=) rs1431897813
NM_144612.6(LOXHD1):c.3293A>G (p.Asn1098Ser) rs876657494
NM_144612.6(LOXHD1):c.3426G>A (p.Val1142=) rs200068167
NM_144612.6(LOXHD1):c.3449A>G (p.Gln1150Arg) rs201576880
NM_144612.6(LOXHD1):c.3471C>T (p.Gly1157=) rs727503141
NM_144612.6(LOXHD1):c.3561G>A (p.Lys1187=) rs376334860
NM_144612.6(LOXHD1):c.3654C>T
NM_144612.6(LOXHD1):c.3672C>T (p.Asp1224=) rs876657495
NM_144612.6(LOXHD1):c.3816G>A (p.Thr1272=) rs1031241585
NM_144612.6(LOXHD1):c.3846C>T (p.Asn1282=) rs759329010
NM_144612.6(LOXHD1):c.3855C>T (p.Asp1285=) rs876657496
NM_144612.6(LOXHD1):c.3936C>G (p.Leu1312=) rs533251927
NM_144612.6(LOXHD1):c.3999C>T (p.Cys1333=) rs117297079
NM_144612.6(LOXHD1):c.4068G>A (p.Arg1356=) rs539688337
NM_144612.6(LOXHD1):c.4089C>T (p.Ile1363=) rs370376314
NM_144612.6(LOXHD1):c.4147A>G (p.Thr1383Ala) rs1182325987
NM_144612.6(LOXHD1):c.4149G>A (p.Thr1383=) rs373657978
NM_144612.6(LOXHD1):c.4212+14T>G rs1555672903
NM_144612.6(LOXHD1):c.4217C>T (p.Ala1406Val) rs146739496
NM_144612.6(LOXHD1):c.4497A>G (p.Ser1499=) rs876657497
NM_144612.6(LOXHD1):c.4523G>A (p.Arg1508Lys) rs199518750
NM_144612.6(LOXHD1):c.4530+107A>G rs1450425
NM_144612.6(LOXHD1):c.4611C>T (p.Cys1537=) rs189561302
NM_144612.6(LOXHD1):c.4671G>A (p.Leu1557=) rs763078543
NM_144612.6(LOXHD1):c.4680C>T (p.Cys1560=) rs397517863
NM_144612.6(LOXHD1):c.4720G>A (p.Glu1574Lys) rs78427072
NM_144612.6(LOXHD1):c.4734C>T (p.Tyr1578=) rs376338995
NM_144612.6(LOXHD1):c.4740+13G>T rs570127242
NM_144612.6(LOXHD1):c.4822G>A (p.Val1608Ile) rs140042576
NM_144612.6(LOXHD1):c.4824C>G (p.Val1608=) rs114557260
NM_144612.6(LOXHD1):c.4842C>T (p.Thr1614=) rs779714173
NM_144612.6(LOXHD1):c.4923G>A (p.Ala1641=) rs761707142
NM_144612.6(LOXHD1):c.5023C>T (p.Arg1675Cys) rs201060702
NM_144612.6(LOXHD1):c.5028C>T (p.Gly1676=) rs865871778
NM_144612.6(LOXHD1):c.5050G>A (p.Ala1684Thr) rs376122149
NM_144612.6(LOXHD1):c.5085+1014G>A rs114014042
NM_144612.6(LOXHD1):c.5085+830C>T rs375851293
NM_144612.6(LOXHD1):c.5085+902C>T rs114736976
NM_144612.6(LOXHD1):c.5103G>A (p.Thr1701=) rs727503138
NM_144612.6(LOXHD1):c.512-5C>T rs1555686876
NM_144612.6(LOXHD1):c.5127C>T (p.Gly1709=) rs373924055
NM_144612.6(LOXHD1):c.51C>T
NM_144612.6(LOXHD1):c.5214-3C>T rs528236655
NM_144612.6(LOXHD1):c.5398C>T (p.Arg1800Trp) rs201994383
NM_144612.6(LOXHD1):c.5503C>T (p.Leu1835=) rs202043044
NM_144612.6(LOXHD1):c.5616C>A (p.Asn1872Lys) rs61733519
NM_144612.6(LOXHD1):c.5667G>A (p.Lys1889=) rs201366522
NM_144612.6(LOXHD1):c.5725G>A (p.Asp1909Asn) rs727504544
NM_144612.6(LOXHD1):c.5864-15C>T rs397517864
NM_144612.6(LOXHD1):c.5886G>A (p.Thr1962=) rs1376734175
NM_144612.6(LOXHD1):c.5898C>T (p.Gly1966=) rs779218726
NM_144612.6(LOXHD1):c.5913C>T (p.Asn1971=) rs146200756
NM_144612.6(LOXHD1):c.5962A>G (p.Met1988Val) rs141749060
NM_144612.6(LOXHD1):c.6057T>C (p.Cys2019=) rs199645176
NM_144612.6(LOXHD1):c.6083G>A
NM_144612.6(LOXHD1):c.6147C>T (p.Tyr2049=) rs374858340
NM_144612.6(LOXHD1):c.6153T>C (p.Asn2051=) rs181548456
NM_144612.6(LOXHD1):c.6156-15C>T rs1354633431
NM_144612.6(LOXHD1):c.6192G>A (p.Lys2064=) rs876657498
NM_144612.6(LOXHD1):c.6276C>G (p.Val2092=) rs141737883
NM_144612.6(LOXHD1):c.6465C>T (p.Arg2155=) rs1057521570
NM_144612.6(LOXHD1):c.6555C>T (p.Ala2185=) rs189873733
NM_144612.6(LOXHD1):c.670A>C (p.Ile224Leu) rs876657499
NM_144612.6(LOXHD1):c.710A>G (p.Asn237Ser) rs539278802
NM_144612.6(LOXHD1):c.717C>T (p.Gly239=) rs1555686141
NM_144612.6(LOXHD1):c.759+11C>T rs755171381
NM_144612.6(LOXHD1):c.87G>A
NM_144612.6(LOXHD1):c.927G>T (p.Gly309=) rs749677224
NM_144612.6(LOXHD1):c.977A>G (p.Asn326Ser) rs188528174

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