NM_004560.4(ROR2):c.937+10C>T AND multiple conditions

Germline classification:: Likely benign (1 submission)
Last evaluated:: Jul 23, 2021
Review status:: 1 star out of maximum of 4 stars
criteria provided, single submitter

Somatic classification of clinical impact:: None
Review status:: (0/4) 0 stars out of maximum of 4 stars
no assertion criteria provided

Somatic classification of oncogenicity:: None
Review status:: (0/4) 0 stars out of maximum of 4 stars
no assertion criteria provided

Record status:: current
Accession:: RCV002500510.1

Allele description [Variation Report for NM_004560.4(ROR2):c.937+10C>T]

NM_004560.4(ROR2):c.937+10C>T

Gene:

ROR2:receptor tyrosine kinase like orphan receptor 2 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

9q22.31

Genomic location:

Preferred name:

NM_004560.4(ROR2):c.937+10C>T

HGVS:

NC_000009.12:g.91733112G>A
NG_008089.1:g.222051C>T
NM_001318204.2:c.937+10C>T
NM_004560.4:c.937+10C>TMANE SELECT
NC_000009.11:g.94495394G>A
NM_004560.3:c.937+10C>T

Links:

dbSNP: rs201083970

Molecular consequence:

NM_001318204.2:c.937+10C>T - intron variant - [Sequence Ontology: SO:0001627]
NM_004560.4:c.937+10C>T - intron variant - [Sequence Ontology: SO:0001627]

Condition(s)

Name:: Brachydactyly type B1 (BDB1)
Identifiers:: MONDO: MONDO:0007220; MedGen: C1862112; Orphanet: 93383; OMIM: 113000

Name:: Autosomal recessive Robinow syndrome (RRS1)
Synonyms:: COSTOVERTEBRAL SEGMENTATION DEFECT WITH MESOMELIA; COVESDEM SYNDROME; ROBINOW SYNDROME, AUTOSOMAL RECESSIVE 1; See all synonyms [MedGen]
Identifiers:: MONDO: MONDO:0009999; MedGen: C5399974; Orphanet: 1507; Orphanet: 97360; OMIM: 268310

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV002811170	Fulgent Genetics, Fulgent Genetics	criteria provided, single submitter (ACMG Guidelines, 2015)	Likely benign (Jul 23, 2021)	unknown	clinical testing	PubMed (1) [See all records that cite this PMID]

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV002811170

Fulgent Genetics, Fulgent Genetics

criteria provided, single submitter

(ACMG Guidelines, 2015)

Likely benign
(Jul 23, 2021)

unknown

clinical testing

PubMed (1)
[See all records that cite this PMID]

Help

Summary from all submissions

Ethnicity	Origin	Affected	Individuals	Families	Chromosomes tested	Number Tested	Family history	Method
not provided	unknown	unknown	not provided	not provided	not provided	not provided	not provided	clinical testing

Citations

PubMed

Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology.

Richards S, Aziz N, Bale S, Bick D, Das S, Gastier-Foster J, Grody WW, Hegde M, Lyon E, Spector E, Voelkerding K, Rehm HL; ACMG Laboratory Quality Assurance Committee.

Genet Med. 2015 May;17(5):405-24. doi: 10.1038/gim.2015.30. Epub 2015 Mar 5.

PubMed [citation]

PMID:: 25741868
PMCID:: PMC4544753

Details of each submission

From Fulgent Genetics, Fulgent Genetics, SCV002811170.1

#	Ethnicity	Individuals	Chromosomes Tested	Family History	Method	Citations
1	not provided	not provided	not provided	not provided	clinical testing	PubMed (1)

#	Sample				Method		Observation
#	Origin	Affected	Number tested	Tissue	Purpose	Method	Individuals	Allele frequency	Families	Co-occurrences
1	unknown	unknown	not provided	not provided	not provided		not provided	not provided	not provided	not provided

Last Updated: Apr 12, 2026

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