rs73569323 Rat Genome Database

rs73569323 Rat Genome Database

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Variant: rs73569323 - Homo sapiens

RGD ID:

150503401

RS ID:

rs73569323

ClinVar ID:

CV1285749

Genic Status:

GENIC

Type:

SNV (SO:0001483)

Associated Genes:

MAF WWOX

Reference Nucleotide:

C

Variant Nucleotide:

T

Position

Assembly	Chr	Position
GRCh37	16	79,245,765
GRCh38	16	79,211,868

JBrowse:

View Region in Genome Browser (JBrowse)

Model

HGVS Name(s)	Last Evaluated	Molecular Consequence	Clinical Significance	Trait Synonyms
NM_001291997.2:c.72C>T NM_016373.4:c.72C>T NG_011698.1:g.1117215C>T NC_000016.10:g.79211868C>T NC_000016.9:g.79245765C>T More...	06/14/2018	3 prime utr variant	benign	none provided

Gene Symbol:	WWOX
Accession:	NM_016373
Location:	3UTRS;EXON

Gene Symbol:	WWOX
Accession:	NM_001291997
Location:	3UTRS;EXON

Gene Symbol:	MAF
Accession:	XM_024450279
Location:	3UTRS;EXON

Gene Symbol:	MAF
Accession:	XR_001751902
Location:	EXON;NON-CODING

Gene Symbol:	MAF
Accession:	XR_002957804
Location:	EXON;NON-CODING

Gene Symbol:	MAF
Accession:	XR_002957803
Location:	EXON;NON-CODING

Gene Symbol:	MAF
Accession:	XR_002957802
Location:	EXON;NON-CODING

Gene Symbol:	WWOX
Accession:	NM_130791
Location:	INTRON

Gene Symbol:	MAF
Accession:	NM_005360
Location:	INTRON

Gene Symbol:	MAF
Accession:	NM_001031804
Location:	INTRON

Gene Symbol:	MAF
Accession:	XM_017023234
Location:	INTRON

Gene Symbol:	MAF
Accession:	XM_017023235
Location:	INTRON

Gene Symbol:	MAF
Accession:	XM_017023233
Location:	INTRON

Gene Symbol:	WWOX
Accession:	NR_120436
Location:	INTRON;NON-CODING

Gene Symbol:	WWOX
Accession:	NR_120435
Location:	INTRON;NON-CODING

ClinVar GRCh37	ClinVar GRCh38

PMID:25741868

Database	Acc Id	Source(s)
ClinVar	RCV001719172	CLINVAR
dbSNP (RS)	rs73569323	CLINVAR
MedGen	C3661900	CLINVAR
NCBI Gene	MAF	CLINVAR
	WWOX	CLINVAR
OMIM	177075	CLINVAR
	605131	CLINVAR