ClinVar Miner

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

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Gene type:
ClinVar version:
Total variants: 36
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HGVS dbSNP
GRCh37/hg19 4p16.2(chr4:5731518-5778783)x1
NM_153717.3(EVC):c.1098+123A>G rs13143108
NM_153717.3(EVC):c.1099-167G>C rs6810769
NM_153717.3(EVC):c.1099-208C>A rs6812234
NM_153717.3(EVC):c.1099-208C>T rs6812234
NM_153717.3(EVC):c.1315+271C>T rs11731603
NM_153717.3(EVC):c.1316-139G>C rs7660793
NM_153717.3(EVC):c.1316-220G>A rs752061
NM_153717.3(EVC):c.1464+177T>A rs2302074
NM_153717.3(EVC):c.1464+236G>T rs9637548
NM_153717.3(EVC):c.1465-285A>G rs12499446
NM_153717.3(EVC):c.1563+185A>G rs12499655
NM_153717.3(EVC):c.174+238T>A rs3755844
NM_153717.3(EVC):c.1776+206C>G rs2878427
NM_153717.3(EVC):c.1855G>A (p.Val619Ile) rs111293777
NM_153717.3(EVC):c.1886+172C>A rs4689303
NM_153717.3(EVC):c.1886+202G>C rs41269561
NM_153717.3(EVC):c.1886+253C>T rs13103000
NM_153717.3(EVC):c.1886+266G>A rs13101471
NM_153717.3(EVC):c.1887-122G>A rs2291152
NM_153717.3(EVC):c.2097+111A>C rs76138881
NM_153717.3(EVC):c.2449+317A>T rs7694192
NM_153717.3(EVC):c.2561+144G>T rs62297684
NM_153717.3(EVC):c.2561+221A>G rs2279251
NM_153717.3(EVC):c.2782+103C>T rs3733185
NM_153717.3(EVC):c.2782+145G>T rs28722043
NM_153717.3(EVC):c.2782+173G>T rs113039000
NM_153717.3(EVC):c.2894+248A>T rs2279249
NM_153717.3(EVC):c.2895-114A>G rs2279247
NM_153717.3(EVC):c.2895-249T>C rs2279248
NM_153717.3(EVC):c.300+213C>T rs4539985
NM_153717.3(EVC):c.301-80G>A rs2276875
NM_153717.3(EVC):c.385-170T>A rs28718969
NM_153717.3(EVC):c.780G>A (p.Lys260=) rs41269555
NM_153717.3(EVC):c.802-311T>C rs1351357
NM_153717.3(EVC):c.939+224C>T rs1001180

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