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rs121913558

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs121913558(A;T)
Make rs121913558(T;T)
ReferenceGRCh38 38.1/141
Chromosome18
Position60372178
GeneMC4R
is asnp
is mentioned by
dbSNPrs121913558
ebirs121913558
HLIrs121913558
Exacrs121913558
Varsomers121913558
Maprs121913558
PheGenIrs121913558
hapmaprs121913558
1000 genomesrs121913558
hgdprs121913558
ensemblrs121913558
gopubmedrs121913558
geneviewrs121913558
scholarrs121913558
googlers121913558
pharmgkbrs121913558
gwascentralrs121913558
openSNPrs121913558
23andMers121913558
23andMe allrs121913558
SNP Nexus

SNPshotrs121913558
SNPdbers121913558
MSV3drs121913558
GWAS Ctlgrs121913558
Max Magnitude0
ClinVar
Risk rs121913558(T;T)
Alt rs121913558(T;T)
Reference rs121913558(A;A)
Significance Pathogenic
Disease Obesity
Variation info
Gene MC4R
CLNDBN Obesity
Reversed 1
HGVS NC_000018.9:g.58039411T>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000015397.25,