ClinVar Miner

Variants in gene ROR2 with conflicting interpretations "likely benign" and "uncertain significance"

Submission 1 (likely benign) minimum review status: Submission 1 (likely benign) method:
Submission 2 (uncertain significance) minimum review status: Submission 2 (uncertain significance) method:
Gene type:
ClinVar version:
Total variants with conflicting interpretations: 31
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HGVS dbSNP gnomAD frequency
NM_004560.4(ROR2):c.2285C>T (p.Ser762Leu) rs34491822 0.00357
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.234G>A (p.Thr78=) rs141093530 0.00046
NM_004560.4(ROR2):c.730C>T (p.Arg244Trp) rs148340413 0.00035
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.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.2445G>A (p.Pro815=) rs202010959 0.00006
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.2805C>G (p.Asp935Glu) rs41277835
NM_004560.4(ROR2):c.623-11G>A rs1350375399

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