ClinVar Miner

Variants in gene ROR2 with conflicting interpretations

Y axis minimum submission review status: Y axis collection method:
X axis minimum submission review status: X axis collection method:
Minimum conflict level:
Gene type:
ClinVar version:

If a variant has more than two submissions, it may have multiple conflicts and therefore be counted in more than one conflict column. If this is the case, the "Variants with any kind of conflict" cell will be less than the sum of the conflicted variants cells to its left.

Variants with only 1 submission per condition Variants with at least 2 submissions on the same condition and no conflicts Variants with a synonymous conflict
(e.g. benign vs non-pathogenic)
Variants with a confidence conflict
(e.g. benign vs likely benign)
Variants with a benign or likely benign vs uncertain conflict Variants with a category conflict
(e.g. benign vs affects)
Variants with a clinically significant conflict
(e.g. benign vs pathogenic)
Variants with any conflict
552 72 0 17 35 0 3 49

Significance breakdown #

In the table below, cells that correspond to a term paired with itself represent synonymous conflicts, i.e. variants that have been annotated with different terms that map to the same standard term. To compare the terms that were actually submitted, check the box in the filters section at the top of this page.

likely pathogenic uncertain significance likely benign benign
likely pathogenic 0 3 1 0
uncertain significance 3 0 33 4
likely benign 1 33 0 17
benign 0 4 17 0

All variants with conflicting interpretations #

Total variants: 49
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_004560.4(ROR2):c.2455G>A (p.Val819Ile) rs10761129 0.71630
NM_004560.4(ROR2):c.733A>G (p.Thr245Ala) rs10820900 0.66416
NM_004560.4(ROR2):c.1710G>A (p.Pro570=) rs41277837 0.02804
NM_004560.4(ROR2):c.75G>A (p.Leu25=) rs148237260 0.01389
NM_004560.4(ROR2):c.-91G>A rs141262722 0.00898
NM_004560.4(ROR2):c.717C>T (p.Cys239=) rs56302651 0.00597
NM_004560.4(ROR2):c.2285C>T (p.Ser762Leu) rs34491822 0.00357
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.372C>T (p.Asp124=) rs145568368 0.00241
NM_004560.4(ROR2):c.2395C>T (p.Pro799Ser) rs141235720 0.00173
NM_004560.4(ROR2):c.1583G>A (p.Arg528Gln) rs142215888 0.00108
NM_004560.4(ROR2):c.1670C>T (p.Ser557Leu) rs56099091 0.00098
NM_004560.4(ROR2):c.1736A>T (p.Asp579Val) rs150610444 0.00092
NM_004560.4(ROR2):c.2461G>A (p.Val821Ile) rs149056068 0.00086
NM_004560.4(ROR2):c.234G>A (p.Thr78=) rs141093530 0.00046
NM_004560.4(ROR2):c.730C>T (p.Arg244Trp) rs148340413 0.00035
NM_004560.4(ROR2):c.751C>T (p.Leu251=) rs368471121 0.00025
NM_004560.4(ROR2):c.1671G>A (p.Ser557=) rs201232887 0.00024
NM_004560.4(ROR2):c.1675G>A (p.Gly559Ser) rs117134265 0.00019
NM_004560.4(ROR2):c.568A>G (p.Thr190Ala) rs34574788 0.00019
NM_004560.4(ROR2):c.2694G>C (p.Gln898His) rs141070315 0.00017
NM_004560.4(ROR2):c.2698G>A (p.Ala900Thr) rs202213533 0.00017
NM_004560.4(ROR2):c.380C>T (p.Thr127Met) rs375080866 0.00017
NM_004560.4(ROR2):c.2117G>A (p.Arg706Gln) rs369717474 0.00013
NM_004560.4(ROR2):c.986G>A (p.Ser329Asn) rs371221714 0.00013
NM_004560.4(ROR2):c.2286G>A (p.Ser762=) rs143759440 0.00012
NM_004560.4(ROR2):c.1930G>A (p.Asp644Asn) rs55798732 0.00011
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.1565G>A (p.Arg522Gln) rs201986784 0.00008
NM_004560.4(ROR2):c.1448G>A (p.Arg483Gln) rs767474960 0.00007
NM_004560.4(ROR2):c.2628G>A (p.Thr876=) rs369201767 0.00007
NM_004560.4(ROR2):c.935G>A (p.Arg312His) rs188376581 0.00007
NM_004560.4(ROR2):c.1756G>A (p.Ala586Thr) rs142386294 0.00006
NM_004560.4(ROR2):c.2212C>T (p.Arg738Cys) rs56231927 0.00006
NM_004560.4(ROR2):c.2445G>A (p.Pro815=) rs202010959 0.00006
NM_004560.4(ROR2):c.1712A>G (p.His571Arg) rs376970201 0.00005
NM_004560.4(ROR2):c.2444C>T (p.Pro815Leu) rs770921333 0.00005
NM_004560.4(ROR2):c.822C>T (p.Asn274=) rs140557090 0.00005
NM_004560.4(ROR2):c.2080T>C (p.Cys694Arg) rs142386992 0.00003
NM_004560.4(ROR2):c.51C>A (p.Ala17=) rs886043361 0.00003
NM_004560.4(ROR2):c.1236C>T (p.Ile412=) rs752218712 0.00002
NM_004560.4(ROR2):c.1054A>G (p.Ser352Gly) rs569242465 0.00001
NM_004560.4(ROR2):c.1970G>A (p.Arg657His) rs529829552 0.00001
NM_004560.4(ROR2):c.2239C>T (p.Arg747Ter) rs374646337 0.00001
NM_004560.4(ROR2):c.2805C>G (p.Asp935Glu) rs41277835
NM_004560.4(ROR2):c.298G>A (p.Ala100Thr) rs374692105
NM_004560.4(ROR2):c.623-11G>A rs1350375399

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.