ClinVar Miner

List of variants in gene CRB2 reported as benign for not provided

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Gene type:
ClinVar version:
Total variants: 109
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HGVS dbSNP gnomAD frequency
NM_173689.7(CRB2):c.269C>A (p.Thr90Asn) rs2808415 0.99946
NM_173689.7(CRB2):c.2126T>C (p.Val709Ala) rs2488602 0.99940
NM_173689.7(CRB2):c.2905A>G (p.Thr969Ala) rs2488601 0.97669
NM_173689.7(CRB2):c.3634-156T>C rs2797947 0.96212
NM_173689.7(CRB2):c.3389+48A>G rs2488599 0.42611
NM_173689.7(CRB2):c.3634-52G>A rs10760283 0.40679
NM_173689.7(CRB2):c.2523G>A (p.Thr841=) rs61740213 0.39220
NM_173689.7(CRB2):c.434T>C (p.Met145Thr) rs1105223 0.37561
NM_173689.7(CRB2):c.419-198A>G rs1105224 0.37213
NM_173689.7(CRB2):c.754+34G>C rs11790447 0.34153
NM_173689.7(CRB2):c.3633+243C>G rs4838054 0.33643
NM_173689.7(CRB2):c.95-169T>C rs56366974 0.32581
NM_173689.7(CRB2):c.476G>C (p.Gly159Ala) rs1105222 0.32311
NM_173689.7(CRB2):c.3390-170_3390-169insA rs35902524 0.31893
NM_173689.7(CRB2):c.755-100G>A rs10760281 0.30266
NM_173689.7(CRB2):c.754+315G>A rs12552768 0.30032
NM_173689.7(CRB2):c.993C>T (p.Asn331=) rs10818812 0.29309
NM_173689.7(CRB2):c.1055-58T>C rs7034379 0.23171
NM_173689.7(CRB2):c.1587G>A (p.Ala529=) rs33984675 0.22033
NM_173689.7(CRB2):c.2076C>T (p.Ser692=) rs13290763 0.21944
NM_173689.7(CRB2):c.3126G>C (p.Ala1042=) rs2488600 0.21017
NM_173689.7(CRB2):c.3634-199C>T rs4838055 0.17824
NM_173689.7(CRB2):c.3633+54G>A rs4838053 0.17195
NC_000009.12:g.123356133G>A rs10985983 0.15971
NM_173689.7(CRB2):c.2437-224G>T rs12342024 0.14637
NM_173689.7(CRB2):c.2436+181C>T rs13291617 0.12832
NM_173689.7(CRB2):c.3329C>T (p.Thr1110Met) rs73571431 0.12417
NM_173689.7(CRB2):c.3633+224A>G rs67785297 0.12167
NM_173689.7(CRB2):c.3506+111T>A rs2797949 0.10682
NM_173689.7(CRB2):c.3021T>C (p.Ala1007=) rs7848449 0.10131
NM_173689.7(CRB2):c.3507-133C>T rs12378884 0.08881
NM_173689.7(CRB2):c.754+9G>A rs4838052 0.07512
NM_173689.7(CRB2):c.940+55C>G rs2797951 0.07324
NM_173689.7(CRB2):c.61C>T (p.Leu21=) rs12551047 0.05364
NM_173689.7(CRB2):c.755-305C>T rs12552775 0.05268
NM_173689.7(CRB2):c.1920C>T (p.Cys640=) rs55965026 0.03935
NM_173689.7(CRB2):c.3389+263T>C rs114763962 0.03789
NM_173689.7(CRB2):c.1054+177T>C rs116294669 0.03218
NM_173689.7(CRB2):c.418+261T>G rs73571408 0.02660
NM_173689.7(CRB2):c.419-16C>A rs73571416 0.02263
NM_173689.7(CRB2):c.94+287G>C rs73569276 0.02258
NM_173689.7(CRB2):c.755-10_755-7dup rs148932652 0.02250
NM_173689.7(CRB2):c.2680G>A (p.Gly894Ser) rs144714250 0.01838
NM_173689.7(CRB2):c.2436+185C>A rs142485768 0.01656
NM_173689.7(CRB2):c.3507-14C>A rs115981769 0.01081
NM_173689.7(CRB2):c.2376G>T (p.Glu792Asp) rs75370841 0.00850
NM_173689.7(CRB2):c.2130G>A (p.Pro710=) rs34057024 0.00697
NM_173689.7(CRB2):c.1828C>T (p.Arg610Trp) rs145286619 0.00688
NM_173689.7(CRB2):c.2709C>T (p.Arg903=) rs116379540 0.00679
NM_173689.7(CRB2):c.137C>T (p.Pro46Leu) rs73571404 0.00665
NM_173689.7(CRB2):c.614+13C>T rs376610848 0.00614
NM_173689.7(CRB2):c.3325C>G (p.His1109Asp) rs185968694 0.00575
NM_173689.7(CRB2):c.278G>A (p.Arg93His) rs138381817 0.00563
NM_173689.7(CRB2):c.205C>T (p.Arg69Trp) rs36035964 0.00556
NM_173689.7(CRB2):c.1055-13G>A rs7021276 0.00538
NM_173689.7(CRB2):c.2748C>T (p.Ala916=) rs372726074 0.00422
NM_173689.7(CRB2):c.1927+10A>T rs137881241 0.00414
NM_173689.7(CRB2):c.1428T>G (p.Thr476=) rs142345530 0.00412
NM_173689.7(CRB2):c.5C>T (p.Ala2Val) rs201425854 0.00326
NM_173689.7(CRB2):c.940+16G>C rs200215866 0.00307
NM_173689.7(CRB2):c.1236C>T (p.Ile412=) rs55641439 0.00277
NM_173689.7(CRB2):c.2112G>A (p.Arg704=) rs114090190 0.00269
NM_173689.7(CRB2):c.1464G>A (p.Leu488=) rs145392563 0.00244
NM_173689.7(CRB2):c.2817G>C (p.Leu939=) rs148565778 0.00240
NM_173689.7(CRB2):c.270C>T (p.Thr90=) rs140031022 0.00223
NM_173689.7(CRB2):c.468G>A (p.Leu156=) rs146419635 0.00222
NM_173689.7(CRB2):c.2789C>T (p.Ala930Val) rs561402183 0.00178
NM_173689.7(CRB2):c.2496C>A (p.Thr832=) rs148249926 0.00155
NM_173689.7(CRB2):c.142G>A (p.Ala48Thr) rs200283870 0.00143
NM_173689.7(CRB2):c.3204C>T (p.Asp1068=) rs377347664 0.00141
NM_173689.7(CRB2):c.3471C>T (p.Ala1157=) rs61745393 0.00130
NM_173689.7(CRB2):c.606G>A (p.Leu202=) rs201174974 0.00130
NM_173689.7(CRB2):c.3738G>C (p.Leu1246=) rs142743710 0.00129
NM_173689.7(CRB2):c.3633+17G>T rs74351477 0.00098
NM_173689.7(CRB2):c.2668G>A (p.Gly890Arg) rs144760112 0.00086
NM_173689.7(CRB2):c.516C>T (p.Cys172=) rs146687164 0.00083
NM_173689.7(CRB2):c.418+8C>T rs201651061 0.00056
NM_173689.7(CRB2):c.2961C>T (p.Arg987=) rs760240136 0.00051
NM_173689.7(CRB2):c.3746G>A (p.Arg1249Gln) rs147412276 0.00045
NM_173689.7(CRB2):c.2043C>T (p.Ser681=) rs151243935 0.00041
NM_173689.7(CRB2):c.755-19C>T rs370972340 0.00039
NM_173689.7(CRB2):c.3634-14C>T rs368619846 0.00035
NM_173689.7(CRB2):c.1429C>T (p.Arg477Cys) rs146271715 0.00024
NM_173689.7(CRB2):c.1062A>T (p.Thr354=) rs191927047 0.00022
NM_173689.7(CRB2):c.1217C>T (p.Pro406Leu) rs34802652 0.00021
NM_173689.7(CRB2):c.946G>A (p.Asp316Asn) rs201386154 0.00021
NM_173689.7(CRB2):c.3466G>A (p.Ala1156Thr) rs201603014 0.00014
NM_173689.7(CRB2):c.765C>T (p.Gly255=) rs138090939 0.00007
NM_173689.7(CRB2):c.3189G>C (p.Ser1063=) rs758441594 0.00004
NC_000009.12:g.123356192G>T rs35454517
NM_173689.7(CRB2):c.-21CAGAGCG[1] rs60364866
NM_173689.7(CRB2):c.1586C>T (p.Ala529Val)
NM_173689.7(CRB2):c.2004C>T (p.Pro668=)
NM_173689.7(CRB2):c.2436+17GGT[5] rs748183673
NM_173689.7(CRB2):c.3389+22dup rs534788085
NM_173689.7(CRB2):c.3390-235G>C rs13288149
NM_173689.7(CRB2):c.3484C>T (p.Leu1162=)
NM_173689.7(CRB2):c.3507-12del
NM_173689.7(CRB2):c.755-210del rs3050063
NM_173689.7(CRB2):c.755-210dup rs3050063
NM_173689.7(CRB2):c.755-211_755-210del rs3050063
NM_173689.7(CRB2):c.755-211_755-210dup rs3050063
NM_173689.7(CRB2):c.755-70C>G rs28647836
NM_173689.7(CRB2):c.883G>T (p.Ala295Ser) rs74778545
NM_173689.7(CRB2):c.905C>T (p.Ala302Val)
NM_173689.7(CRB2):c.940+100_940+106del rs68008388
NM_173689.7(CRB2):c.940+72A>C rs150634227
NM_173689.7(CRB2):c.940+79_940+80del rs10537052
NM_173689.7(CRB2):c.941-100CT[3] rs201080656

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