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rs121913567

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121913567(C;T)
Make rs121913567(T;T)
ReferenceGRCh38 38.1/141
Chromosome18
Position60371694
GeneMC4R
is asnp
is mentioned by
dbSNPrs121913567
ebirs121913567
HLIrs121913567
Exacrs121913567
Varsomers121913567
Maprs121913567
PheGenIrs121913567
hapmaprs121913567
1000 genomesrs121913567
hgdprs121913567
ensemblrs121913567
gopubmedrs121913567
geneviewrs121913567
scholarrs121913567
googlers121913567
pharmgkbrs121913567
gwascentralrs121913567
openSNPrs121913567
23andMers121913567
23andMe allrs121913567
SNP Nexus

SNPshotrs121913567
SNPdbers121913567
MSV3drs121913567
GWAS Ctlgrs121913567
Max Magnitude0
ClinVar
Risk rs121913567(T;T)
Alt rs121913567(T;T)
Reference rs121913567(C;C)
Significance Pathogenic
Disease Obesity
Variation info
Gene MC4R
CLNDBN Obesity
Reversed 1
HGVS NC_000018.9:g.58038927G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000015414.21,