rs74315349

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(C;C)	0	common in clinvar

Make rs74315349(C;T)

Make rs74315349(T;T)

Reference

GRCh38 38.1/141

Chromosome

1

Position

26913841

Gene	NR0B2, NUDC

is a	snp
is	mentioned by
dbSNP	rs74315349
dbSNP (classic)	rs74315349
ClinGen	rs74315349
ebi	rs74315349
HLI	rs74315349
Exac	rs74315349
Gnomad	rs74315349
Varsome	rs74315349
LitVar	rs74315349
Map	rs74315349
PheGenI	rs74315349
Biobank	rs74315349
1000 genomes	rs74315349
hgdp	rs74315349
ensembl	rs74315349
geneview	rs74315349
scholar	rs74315349
google	rs74315349
pharmgkb	rs74315349
gwascentral	rs74315349
openSNP	rs74315349
23andMe	rs74315349
SNPshot	rs74315349
SNPdbe	rs74315349
MSV3d	rs74315349
GWAS Ctlg	rs74315349

Max Magnitude

0

OMIM	604630
Desc
Variant	0001
Related	also

ClinVar
Risk	rs74315349(G;G) rs74315349(T;T)
Alt	rs74315349(G;G) rs74315349(T;T)
Reference	Rs74315349(C;C)
Significance	Pathogenic
Disease	Obesity
Variation	info
Gene	NR0B2
CLNDBN	Obesity, mild, early-onset
Reversed	1
HGVS	NC_000001.10:g.27240332G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000005759.2,