ClinVar Miner

List of variants in gene DNM2 reported as benign for not provided

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Gene type:
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Total variants: 45
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HGVS dbSNP gnomAD frequency
NM_001005361.3(DNM2):c.992+231G>A rs8102648 0.93725
NM_001005361.3(DNM2):c.236-29C>G rs3826803 0.56569
NM_001005361.3(DNM2):c.1128+158G>C rs1610095 0.52451
NM_001005361.3(DNM2):c.1128+169T>C rs2278444 0.34249
NM_001005361.3(DNM2):c.386-173G>T rs4804528 0.32115
NM_001005361.3(DNM2):c.2139T>C (p.Ala713=) rs2229920 0.30148
NM_001005361.3(DNM2):c.1893+248T>C rs67417605 0.29061
NM_001005361.3(DNM2):c.*268A>T rs12461992 0.17591
NM_001005361.3(DNM2):c.2058+262A>G rs12973986 0.15029
NM_001005361.3(DNM2):c.1545+41C>T rs2287029 0.12846
NM_001005361.3(DNM2):c.1893+31_1893+32insC rs138202845 0.06030
NM_001005361.3(DNM2):c.2292-85A>G rs58724234 0.05980
NM_001005361.3(DNM2):c.2058+89G>A rs57561584 0.05640
NM_001005361.3(DNM2):c.161+228C>G rs113305450 0.05468
NM_001005361.3(DNM2):c.1077C>T (p.Gly359=) rs112238216 0.02416
NM_001005361.3(DNM2):c.590-168T>C rs10405772 0.02208
NM_001005361.3(DNM2):c.1894-181G>A rs114589854 0.01671
NM_001005361.3(DNM2):c.2484G>A (p.Pro828=) rs114682382 0.01064
NM_001005361.3(DNM2):c.235+12C>A rs147026993 0.00953
NM_001005361.3(DNM2):c.1782-11C>T rs78580529 0.00921
NM_001005361.3(DNM2):c.235+6A>G rs113192269 0.00748
NM_001005361.3(DNM2):c.2543+7C>G rs201979143 0.00364
NM_001005361.3(DNM2):c.236-8C>G rs143084059 0.00361
NM_001005361.3(DNM2):c.519T>C (p.Ala173=) rs77702567 0.00359
NM_001005361.3(DNM2):c.1545+14C>G rs114713494 0.00350
NM_001005361.3(DNM2):c.643G>A (p.Asp215Asn) rs145478270 0.00168
NM_001005361.3(DNM2):c.2160C>T (p.Asp720=) rs117598326 0.00163
NM_001005361.3(DNM2):c.1902C>T (p.Asn634=) rs2229919 0.00149
NM_001005361.3(DNM2):c.386-6T>A rs114623441 0.00118
NM_001005361.3(DNM2):c.1218C>T (p.Asp406=) rs147668465 0.00116
NM_001005361.3(DNM2):c.*10G>A rs200188660 0.00029
NM_001005361.3(DNM2):c.2179C>T (p.His727Tyr) rs142963320 0.00024
NM_001005361.3(DNM2):c.2567G>A (p.Ser856Asn) rs149825590 0.00021
NM_001005361.3(DNM2):c.528C>T (p.Pro176=) rs147579870 0.00015
NM_001005361.3(DNM2):c.2592C>T (p.Ala864=) rs373161548 0.00011
NM_001005361.3(DNM2):c.316G>A (p.Asp106Asn) rs375151459 0.00011
NM_001005361.3(DNM2):c.1377C>T (p.Ile459=) rs369345296 0.00007
NM_001005361.3(DNM2):c.1836C>T (p.Asp612=) rs767061986 0.00002
NM_001005361.3(DNM2):c.2201A>G (p.Asn734Ser) rs577767034 0.00001
NC_000019.10:g.10717821dup rs35784277
NM_001005361.3(DNM2):c.1197-62G>C rs74718485
NM_001005361.3(DNM2):c.1494-43C>G rs2287028
NM_001005361.3(DNM2):c.162-7C>A rs148318860
NM_001005361.3(DNM2):c.235+240dup rs113004875
NM_001005361.3(DNM2):c.590-31CCTCTGA[3] rs748362325

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