ClinVar Miner

List of variants in gene CR2 reported as benign

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Gene type:
ClinVar version:
Total variants: 45
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HGVS dbSNP gnomAD frequency
NM_001006658.3(CR2):c.445+235C>T rs1257562 0.96549
NM_001006658.3(CR2):c.3185C>A (p.Ala1062Glu) rs17617 0.88540
NM_001006658.3(CR2):c.445+88G>T rs1032980 0.67587
NM_001006658.3(CR2):c.59-176C>G rs311311 0.65122
NM_001006658.3(CR2):c.1226-136G>A rs10863322 0.46647
NM_001006658.3(CR2):c.1776G>A (p.Leu592=) rs1048971 0.42495
NM_001006658.3(CR2):c.3113-145C>G rs12032512 0.38172
NM_001006658.3(CR2):c.1987T>C (p.Ser663Pro) rs4308977 0.32718
NM_001006658.3(CR2):c.1571-161C>A rs9429936 0.32010
NM_001006658.3(CR2):c.1571-222G>A rs9429774 0.30796
NM_001006658.3(CR2):c.1916G>A (p.Ser639Asn) rs17615 0.30786
NM_001006658.3(CR2):c.2012G>A (p.Arg671His) rs17616 0.30700
NM_001006658.3(CR2):c.734+51G>A rs1507764 0.17883
NM_001006658.3(CR2):c.3188+46T>A rs17258996 0.15209
NM_001006658.3(CR2):c.2328T>C (p.Ile776=) rs61735651 0.09124
NM_001006658.3(CR2):c.58+97G>A rs1876453 0.08516
NM_001006658.3(CR2):c.3154A>G (p.Ile1052Val) rs17618 0.07668
NM_001006658.3(CR2):c.2240+109A>G rs9429775 0.07128
NM_001006658.3(CR2):c.2324-176C>A rs3991865 0.07081
NM_001006658.3(CR2):c.1617C>T (p.Thr539=) rs34349246 0.02179
NM_001006658.3(CR2):c.2649T>C (p.Gly883=) rs1143665 0.02114
NM_001006658.3(CR2):c.635-20A>T rs17045039 0.00789
NM_001006658.3(CR2):c.445+17A>G rs145095346 0.00786
NM_001006658.3(CR2):c.1622G>T (p.Ser541Ile) rs144075435 0.00520
NM_001006658.3(CR2):c.2240+19A>G rs140933861 0.00357
NM_001006658.3(CR2):c.2352T>C (p.Ile784=) rs142319454 0.00170
NM_001006658.3(CR2):c.2844G>A (p.Glu948=) rs61754518 0.00098
NM_001006658.3(CR2):c.1978+7A>T rs201274951 0.00068
NM_001006658.3(CR2):c.1494-17C>T rs150388945 0.00031
NM_001006658.3(CR2):c.1395A>G (p.Gln465=) rs188078143 0.00029
NM_001006658.3(CR2):c.200C>G (p.Thr67Ser) rs45573035 0.00024
NM_001006658.3(CR2):c.2445A>G (p.Gly815=) rs141282665 0.00024
NM_001006658.3(CR2):c.375C>T (p.Asn125=) rs138096192 0.00018
NM_001006658.3(CR2):c.58+13G>A rs373721952 0.00016
NM_001006658.3(CR2):c.2241-6C>T rs200614122 0.00008
NM_001006658.3(CR2):c.1296A>T (p.Gly432=) rs201585844
NM_001006658.3(CR2):c.2903-171T>C rs61821132
NM_001006658.3(CR2):c.2903-292G>T rs7549152
NM_001006658.3(CR2):c.3089-288TTTTTG[4] rs61547182
NM_001006658.3(CR2):c.3089-3del rs1274247380
NM_001006658.3(CR2):c.3113-217A>C rs2182909
NM_001006658.3(CR2):c.3189-8_3189-7del rs112859639
NM_001006658.3(CR2):c.446-32C>T rs2063143
NM_001006658.3(CR2):c.624C>A (p.Pro208=) rs61759494
NM_001006658.3(CR2):c.624C>G (p.Pro208=) rs61759494

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