ClinVar Miner

List of variants in gene ROR2 reported as benign for not provided

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Total variants: 70
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HGVS dbSNP gnomAD frequency
NM_004560.4(ROR2):c.495-164A>G rs9409459 0.97231
NM_004560.4(ROR2):c.*16G>A rs2230578 0.73170
NM_004560.4(ROR2):c.2455G>A (p.Val819Ile) rs10761129 0.71630
NM_004560.4(ROR2):c.494+25G>A rs12683181 0.68697
NM_004560.4(ROR2):c.733A>G (p.Thr245Ala) rs10820900 0.66416
NM_004560.4(ROR2):c.2088C>T (p.Tyr696=) rs10992063 0.44353
NM_004560.4(ROR2):c.622+55C>T rs7855522 0.42790
NM_004560.4(ROR2):c.937+118C>T rs9409457 0.42419
NM_004560.4(ROR2):c.1387-70G>A rs10992065 0.24992
NM_004560.4(ROR2):c.98-15G>C rs7863557 0.22863
NM_004560.4(ROR2):c.98-288C>T rs10992091 0.22825
NC_000009.12:g.91950449A>T rs114541967 0.12650
NM_004560.4(ROR2):c.97+218A>G rs7045603 0.12536
NM_004560.4(ROR2):c.463+193G>A rs35022100 0.12468
NM_004560.4(ROR2):c.1184-187G>A rs10992066 0.11055
NM_004560.4(ROR2):c.938-33C>T rs10992070 0.09787
NM_004560.4(ROR2):c.498T>C (p.Asp166=) rs16907720 0.09084
NM_004560.4(ROR2):c.495-165C>T rs79766334 0.07882
NM_004560.4(ROR2):c.937+119C>T rs79697373 0.07447
NM_004560.4(ROR2):c.98-67A>G rs3802377 0.06635
NM_004560.4(ROR2):c.98-100G>A rs3802378 0.06633
NM_004560.4(ROR2):c.*712C>T rs1135150 0.05951
NM_004560.4(ROR2):c.2154C>T (p.Pro718=) rs2230577 0.05836
NM_004560.4(ROR2):c.176-115G>A rs60617711 0.05396
NC_000009.12:g.91950467A>C rs3808842 0.04677
NM_004560.4(ROR2):c.1386+233T>C rs7042581 0.04031
NM_004560.4(ROR2):c.623-122C>T rs113031996 0.03716
NM_004560.4(ROR2):c.176-319C>T rs12001678 0.03212
NM_004560.4(ROR2):c.276C>T (p.Asn92=) rs56227711 0.03061
NM_004560.4(ROR2):c.1710G>A (p.Pro570=) rs41277837 0.02804
NM_004560.4(ROR2):c.97+93C>T rs147067450 0.02561
NM_004560.4(ROR2):c.623-22G>A rs73654048 0.02344
NM_004560.4(ROR2):c.623-297del rs148477816 0.01897
NM_004560.4(ROR2):c.1045C>G (p.His349Asp) rs55983376 0.01689
NM_004560.4(ROR2):c.75G>A (p.Leu25=) rs148237260 0.01389
NM_004560.4(ROR2):c.2727G>A (p.Val909=) rs56091954 0.01249
NM_004560.4(ROR2):c.1642C>T (p.Pro548Ser) rs35764413 0.01175
NM_004560.4(ROR2):c.-91G>A rs141262722 0.00898
NM_004560.4(ROR2):c.471G>A (p.Thr157=) rs78781083 0.00812
NM_004560.4(ROR2):c.717C>T (p.Cys239=) rs56302651 0.00597
NM_004560.4(ROR2):c.937+10C>T rs201083970 0.00310
NM_004560.4(ROR2):c.7C>T (p.Arg3Trp) rs539329891 0.00261
NM_004560.4(ROR2):c.175+17A>G rs372392835 0.00243
NM_004560.4(ROR2):c.372C>T (p.Asp124=) rs145568368 0.00241
NM_004560.4(ROR2):c.1686C>T (p.His562=) rs56048121 0.00232
NM_004560.4(ROR2):c.2083G>A (p.Gly695Arg) rs34431454 0.00174
NM_004560.4(ROR2):c.937+16C>T rs112054737 0.00101
NM_004560.4(ROR2):c.2461G>A (p.Val821Ile) rs149056068 0.00086
NM_004560.4(ROR2):c.730C>T (p.Arg244Trp) rs148340413 0.00035
NM_004560.4(ROR2):c.2109G>T (p.Glu703Asp) rs200805854 0.00025
NM_004560.4(ROR2):c.751C>T (p.Leu251=) rs368471121 0.00025
NM_004560.4(ROR2):c.1317G>A (p.Pro439=) rs150661792 0.00014
NM_004560.4(ROR2):c.2399A>C (p.Gln800Pro) rs758757733 0.00014
NM_004560.4(ROR2):c.2466C>T (p.Asn822=) rs146432734 0.00011
NM_004560.4(ROR2):c.744G>A (p.Pro248=) rs757948078 0.00009
NM_004560.4(ROR2):c.485A>G (p.His162Arg) rs569718323 0.00007
NM_004560.4(ROR2):c.2212C>T (p.Arg738Cys) rs56231927 0.00006
NM_004560.4(ROR2):c.1712A>G (p.His571Arg) rs376970201 0.00005
NM_004560.4(ROR2):c.2620G>A (p.Val874Ile) rs200867550 0.00004
NM_004560.4(ROR2):c.1860T>C (p.Asn620=) rs530761262 0.00001
NM_004560.4(ROR2):c.538A>G (p.Ile180Val) rs553341457 0.00001
NM_004560.4(ROR2):c.*170AG[1] rs140581955
NM_004560.4(ROR2):c.1261C>G (p.Leu421Val)
NM_004560.4(ROR2):c.2064C>T (p.Tyr688=)
NM_004560.4(ROR2):c.2805C>G (p.Asp935Glu) rs41277835
NM_004560.4(ROR2):c.2806G>A (p.Glu936Lys)
NM_004560.4(ROR2):c.298G>A (p.Ala100Thr) rs374692105
NM_004560.4(ROR2):c.463+206G>C rs71494474
NM_004560.4(ROR2):c.622+154G>T rs10992073
NM_004560.4(ROR2):c.97+200C>A rs139122017

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