NM_000894.3(LHB):c.183+18del AND Isolated lutropin deficiency

Germline classification:: Benign (1 submission)
Last evaluated:: Aug 19, 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:: RCV001730925.2

Allele description [Variation Report for NM_000894.3(LHB):c.183+18del]

NM_000894.3(LHB):c.183+18del

Gene:

LHB:luteinizing hormone subunit beta [Gene - OMIM - HGNC]

Variant type:

Deletion

Cytogenetic location:

19q13.33

Genomic location:

Preferred name:

NM_000894.3(LHB):c.183+18del

HGVS:

NC_000019.10:g.49016529del
NG_011464.1:g.5562del
NG_033041.1:g.27631del
NM_000894.3:c.183+18delMANE SELECT
LRG_1361t1:c.183+18del
LRG_1361:g.5562del
NC_000019.9:g.49519786del
NM_000894.2:c.183+18del

Links:

dbSNP: rs140502544

NCBI 1000 Genomes Browser:

rs140502544

Molecular consequence:

NM_000894.3:c.183+18del - intron variant - [Sequence Ontology: SO:0001627]

Condition(s)

Name:: Isolated lutropin deficiency (HH23)
Synonyms:: FERTILE EUNUCH SYNDROME; HYPOGONADOTROPIC HYPOGONADISM 23 WITHOUT ANOSMIA; PASQUALINI SYNDROME; See all synonyms [MedGen]
Identifiers:: MONDO: MONDO:0009223; MedGen: C0271582; OMIM: 228300

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV001981357	Genome-Nilou Lab	criteria provided, single submitter (ACMG Guidelines, 2015)	Benign (Aug 19, 2021)	germline	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

SCV001981357

Genome-Nilou Lab

criteria provided, single submitter

(ACMG Guidelines, 2015)

Benign
(Aug 19, 2021)

germline

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	germline	no	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 Genome-Nilou Lab, SCV001981357.1

#	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	germline	no	not provided	not provided	not provided		not provided	not provided	not provided	not provided

Last Updated: Sep 29, 2024

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