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
227 26 0 5 12 0 3 19

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 2 1 0
uncertain significance 2 0 11 1
likely benign 1 11 0 5
benign 0 1 5 0

All variants with conflicting interpretations #

Total variants: 19
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NM_004560.4(ROR2):c.1448G>A (p.Arg483Gln) rs767474960
NM_004560.4(ROR2):c.1675G>A (p.Gly559Ser) rs117134265
NM_004560.4(ROR2):c.1736A>T (p.Asp579Val) rs150610444
NM_004560.4(ROR2):c.1756G>A (p.Ala586Thr) rs142386294
NM_004560.4(ROR2):c.1970G>A (p.Arg657His) rs529829552
NM_004560.4(ROR2):c.2239C>T (p.Arg747Ter) rs374646337
NM_004560.4(ROR2):c.2285C>T (p.Ser762Leu) rs34491822
NM_004560.4(ROR2):c.234G>A (p.Thr78=) rs141093530
NM_004560.4(ROR2):c.2395C>T (p.Pro799Ser) rs141235720
NM_004560.4(ROR2):c.2445G>A (p.Pro815=) rs202010959
NM_004560.4(ROR2):c.2455G>A (p.Val819Ile) rs10761129
NM_004560.4(ROR2):c.2805C>G (p.Asp935Glu) rs41277835
NM_004560.4(ROR2):c.372C>T (p.Asp124=) rs145568368
NM_004560.4(ROR2):c.568A>G (p.Thr190Ala) rs34574788
NM_004560.4(ROR2):c.733A>G (p.Thr245Ala) rs10820900
NM_004560.4(ROR2):c.75G>A (p.Leu25=) rs148237260
NM_004560.4(ROR2):c.7C>T (p.Arg3Trp) rs539329891
NM_004560.4(ROR2):c.937+10C>T rs201083970
NM_004560.4(ROR2):c.986G>A (p.Ser329Asn) rs371221714

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