ClinVar Miner

List of variants in gene LOXHD1 reported as likely benign by PreventionGenetics, part of Exact Sciences

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Total variants: 41
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HGVS dbSNP gnomAD frequency
NM_001384474.1(LOXHD1):c.5802C>A (p.Asn1934Lys) rs61733519 0.00316
NM_001384474.1(LOXHD1):c.1570C>T (p.Arg524Cys) rs192376005 0.00295
NM_001384474.1(LOXHD1):c.1617G>A (p.Met539Ile) rs143142227 0.00178
NM_001384474.1(LOXHD1):c.5313C>T (p.Gly1771=) rs373924055 0.00168
NM_001384474.1(LOXHD1):c.5023C>T (p.Arg1675Cys) rs201060702 0.00149
NM_001384474.1(LOXHD1):c.3024C>T (p.Val1008=) rs370616818 0.00138
NM_001384474.1(LOXHD1):c.177G>A (p.Thr59=) rs116413527 0.00108
NM_001384474.1(LOXHD1):c.3673A>G (p.Ser1225Gly) rs370149278 0.00103
NM_001384474.1(LOXHD1):c.3449A>G (p.Gln1150Arg) rs201576880 0.00088
NM_001384474.1(LOXHD1):c.3941C>T (p.Thr1314Ile) rs182125538 0.00083
NM_001384474.1(LOXHD1):c.4244G>A (p.Arg1415Gln) rs374728484 0.00073
NM_001384474.1(LOXHD1):c.5050G>A (p.Ala1684Thr) rs376122149 0.00063
NM_001384474.1(LOXHD1):c.722A>G (p.Asn241Ser) rs191697915 0.00041
NM_001384474.1(LOXHD1):c.1746G>A (p.Gly582=) rs370933210 0.00028
NM_001384474.1(LOXHD1):c.3453C>T (p.Ser1151=) rs551949683 0.00024
NM_001384474.1(LOXHD1):c.4611C>T (p.Cys1537=) rs189561302 0.00021
NM_001384474.1(LOXHD1):c.6220T>C (p.Leu2074=) rs185604776 0.00018
NM_001384474.1(LOXHD1):c.2655G>A (p.Glu885=) rs371763582 0.00017
NM_001384474.1(LOXHD1):c.1893C>T (p.Ser631=) rs375920647 0.00011
NM_001384474.1(LOXHD1):c.4089C>T (p.Ile1363=) rs370376314 0.00011
NM_001384474.1(LOXHD1):c.2599-10C>T rs751081260 0.00006
NM_001384474.1(LOXHD1):c.3936C>G (p.Leu1312=) rs533251927 0.00006
NM_001384474.1(LOXHD1):c.4149G>A (p.Thr1383=) rs373657978 0.00006
NM_001384474.1(LOXHD1):c.4376-6G>A rs369463541 0.00006
NM_001384474.1(LOXHD1):c.4147A>G (p.Thr1383Ala) rs1182325987 0.00005
NM_001384474.1(LOXHD1):c.131-5T>C rs1028082247 0.00004
NM_001384474.1(LOXHD1):c.2718G>A (p.Val906=) rs765691566 0.00004
NM_001384474.1(LOXHD1):c.5661C>T (p.Tyr1887=) rs1170185905 0.00004
NM_001384474.1(LOXHD1):c.6483A>G (p.Thr2161=) rs568443351 0.00004
NM_001384474.1(LOXHD1):c.2841C>T (p.Asp947=) rs761010290 0.00003
NM_001384474.1(LOXHD1):c.1431+9G>A rs181825231 0.00001
NM_001384474.1(LOXHD1):c.4818C>T (p.Ala1606=) rs976758061 0.00001
NM_001384474.1(LOXHD1):c.5739C>T (p.Asn1913=) rs756448029 0.00001
NM_001384474.1(LOXHD1):c.6516C>T (p.Ala2172=) rs886042223 0.00001
NM_001384474.1(LOXHD1):c.2251C>A (p.Arg751=) rs376539851
NM_001384474.1(LOXHD1):c.3619+9G>A rs576031049
NM_001384474.1(LOXHD1):c.5028C>T (p.Gly1676=) rs865871778
NM_001384474.1(LOXHD1):c.5247C>T (p.Ala1749=)
NM_001384474.1(LOXHD1):c.6182+4G>A
NM_001384474.1(LOXHD1):c.759+11C>T rs755171381
NM_001384474.1(LOXHD1):c.884-4C>A

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