rs1758060204 Rat Genome Database

rs1758060204 Rat Genome Database

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Variant: rs1758060204 - Homo sapiens

RGD ID:

126729130

RS ID:

rs1758060204

ClinVar ID:

CV990834

Genic Status:

GENIC

Type:

SNV (SO:0001483)

Associated Genes:

Reference Nucleotide:

C

Variant Nucleotide:

T

Position

Assembly	Chr	Position
GRCh37	5	160,886,625
GRCh38	5	161,459,619

JBrowse:

View Region in Genome Browser (JBrowse)

Model

HGVS Name(s)	Last Evaluated	Molecular Consequence	Clinical Significance	Trait Synonyms
NM_000813.3:c.458+5G>A NM_001371727.1:c.458+5G>A NM_021911.3:c.458+5G>A NG_047050.1:g.93506G>A More...	03/06/2021	intron variant	likely benign\|uncertain significance	Intellectual developmental disorder; intellectual disabilities; Intellectual functioning disability

Object Symbol	Species	Term	Qualifier	Evidence	With	Reference	Notes	Source	Original Reference(s)
CV990834	Human	intellectual disability		IAGP		8554872	ClinVar Annotator: match by term: Intellectual disability	ClinVar	PMID:28492532

Object Symbol	Species	Term	Qualifier	Evidence	With	Reference	Notes	Source	Original Reference(s)
CV990834	Human	Intellectual disability		IAGP		8554872	ClinVar Annotator: match by term: Intellectual disability	ClinVar	PMID:28492532

Gene Symbol:	GABRB2
Accession:	NM_000813
Location:	INTRON

Gene Symbol:	GABRB2
Accession:	NM_021911
Location:	INTRON

Gene Symbol:	GABRB2
Accession:	NM_001371727
Location:	INTRON

ClinVar GRCh37	ClinVar GRCh38

PMID:28492532

Database	Acc Id	Source(s)
ClinVar	RCV001303518	CLINVAR
dbSNP (RS)	rs1758060204	CLINVAR
MedGen	C3714756	CLINVAR
NCBI Gene	GABRB2	CLINVAR
OMIM	600232	CLINVAR
SNOMED CT	228156007	CLINVAR