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rs74315350

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs74315350(G;T)
Make rs74315350(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position26912036
GeneNR0B2
is asnp
is mentioned by
dbSNPrs74315350
ebirs74315350
HLIrs74315350
Exacrs74315350
Varsomers74315350
Maprs74315350
PheGenIrs74315350
hapmaprs74315350
1000 genomesrs74315350
hgdprs74315350
ensemblrs74315350
gopubmedrs74315350
geneviewrs74315350
scholarrs74315350
googlers74315350
pharmgkbrs74315350
gwascentralrs74315350
openSNPrs74315350
23andMers74315350
23andMe allrs74315350
SNP Nexus

SNPshotrs74315350
SNPdbers74315350
MSV3drs74315350
GWAS Ctlgrs74315350
Max Magnitude0
OMIM604630
Desc
Variant0002
Relatedalso
ClinVar
Risk rs74315350(T;T)
Alt rs74315350(T;T)
Reference rs74315350(G;G)
Significance Pathogenic
Disease Obesity
Variation info
Gene NR0B2
CLNDBN Obesity, mild, early-onset
Reversed 1
HGVS NC_000001.10:g.27238527C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000005760.2,