rs131757 Rat Genome Database

rs131757 Rat Genome Database

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Variant: rs131757 - Homo sapiens

RGD ID:

14707488

RS ID:

rs131757

ClinVar ID:

CV669723

Genic Status:

GENIC

Type:

SNV (SO:0001483)

Associated Genes:

CHKB-DT LOC130067884

Reference Nucleotide:

A

Variant Nucleotide:

C

Position

Assembly	Chr	Position
GRCh37	22	51,021,579
GRCh38	22	50,583,150

JBrowse:

View Region in Genome Browser (JBrowse)

Model

HGVS Name(s)	Last Evaluated	Molecular Consequence	Clinical Significance	Trait Synonyms
NG_029213.1:g.4850T>G NG_012643.1:g.518T>G NC_000022.11:g.50583150A>C NC_000022.10:g.51021579A>C More...	06/18/2018	non-coding transcript variant	benign	none provided; RECLASSIFIED - ADRA2C POLYMORPHISM; RECLASSIFIED - ADRB1 POLYMORPHISM

Gene Symbol:	CHKB-DT
Accession:	NR_021492
Location:	EXON;NON-CODING

Gene Symbol:	CHKB-DT
Accession:	NR_110536
Location:	EXON;NON-CODING

ClinVar GRCh37	ClinVar GRCh38

PMID:25741868

Database	Acc Id	Source(s)
ClinVar	RCV000826860	CLINVAR
dbSNP (RS)	rs131757	CLINVAR
MedGen	C3661900	CLINVAR
NCBI Gene	CHKB	CLINVAR
	CHKB-DT	CLINVAR
	LOC130067884	CLINVAR
OMIM	612395	CLINVAR