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rs13447331

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs13447331(C;T)
Make rs13447331(T;T)
ReferenceGRCh38 38.1/142
Chromosome18
Position60371970
GeneMC4R
is asnp
is mentioned by
dbSNPrs13447331
ebirs13447331
HLIrs13447331
Exacrs13447331
Varsomers13447331
Maprs13447331
PheGenIrs13447331
hapmaprs13447331
1000 genomesrs13447331
hgdprs13447331
ensemblrs13447331
gopubmedrs13447331
geneviewrs13447331
scholarrs13447331
googlers13447331
pharmgkbrs13447331
gwascentralrs13447331
openSNPrs13447331
23andMers13447331
23andMe allrs13447331
SNP Nexus

SNPshotrs13447331
SNPdbers13447331
MSV3drs13447331
GWAS Ctlgrs13447331
Max Magnitude0
OMIM155541
Desc
Variant0021
Relatedalso
ClinVar
Risk rs13447331(T;T)
Alt rs13447331(T;T)
Reference rs13447331(C;C)
Significance Pathogenic
Disease Obesity
Variation info
Gene MC4R
CLNDBN Obesity
Reversed 1
HGVS NC_000018.9:g.58039203G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000015412.26,