Have questions? Visit https://www.reddit.com/r/SNPedia

rs121913565

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs121913565(A;G)
Make rs121913565(G;G)
ReferenceGRCh38 38.1/141
Chromosome18
Position60372061
GeneMC4R
is asnp
is mentioned by
dbSNPrs121913565
ebirs121913565
HLIrs121913565
Exacrs121913565
Varsomers121913565
Maprs121913565
PheGenIrs121913565
hapmaprs121913565
1000 genomesrs121913565
hgdprs121913565
ensemblrs121913565
gopubmedrs121913565
geneviewrs121913565
scholarrs121913565
googlers121913565
pharmgkbrs121913565
gwascentralrs121913565
openSNPrs121913565
23andMers121913565
23andMe allrs121913565
SNP Nexus

SNPshotrs121913565
SNPdbers121913565
MSV3drs121913565
GWAS Ctlgrs121913565
Max Magnitude0
ClinVar
Risk rs121913565(G;G)
Alt rs121913565(G;G)
Reference rs121913565(A;A)
Significance Pathogenic
Disease Obesity
Variation info
Gene MC4R
CLNDBN Obesity
Reversed 1
HGVS NC_000018.9:g.58039294T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000015409.21,