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rs74315349

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs74315349(C;T)
Make rs74315349(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position26913841
GeneNR0B2
is asnp
is mentioned by
dbSNPrs74315349
ebirs74315349
HLIrs74315349
Exacrs74315349
Varsomers74315349
Maprs74315349
PheGenIrs74315349
hapmaprs74315349
1000 genomesrs74315349
hgdprs74315349
ensemblrs74315349
gopubmedrs74315349
geneviewrs74315349
scholarrs74315349
googlers74315349
pharmgkbrs74315349
gwascentralrs74315349
openSNPrs74315349
23andMers74315349
23andMe allrs74315349
SNP Nexus

SNPshotrs74315349
SNPdbers74315349
MSV3drs74315349
GWAS Ctlgrs74315349
Max Magnitude0
OMIM604630
Desc
Variant0001
Relatedalso
ClinVar
Risk rs74315349(G,T;G,T)
Alt rs74315349(G,T;G,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,