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

rs74315393

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in complete genomics
Make rs74315393(A;A)
Make rs74315393(A;T)
ReferenceGRCh38 38.1/141
Chromosome20
Position56249280
GeneMC3R
is asnp
is mentioned by
dbSNPrs74315393
ebirs74315393
HLIrs74315393
Exacrs74315393
Varsomers74315393
Maprs74315393
PheGenIrs74315393
hapmaprs74315393
1000 genomesrs74315393
hgdprs74315393
ensemblrs74315393
gopubmedrs74315393
geneviewrs74315393
scholarrs74315393
googlers74315393
pharmgkbrs74315393
gwascentralrs74315393
openSNPrs74315393
23andMers74315393
23andMe allrs74315393
SNP Nexus

SNPshotrs74315393
SNPdbers74315393
MSV3drs74315393
GWAS Ctlgrs74315393
Max Magnitude0
OMIM155540
Desc
Variant0001
Relatedalso
ClinVar
Risk rs74315393(A;A)
Alt rs74315393(A;A)
Reference rs74315393(T;T)
Significance Other
Disease Body mass index quantitative trait locus 9
Variation info
Gene MC3R
CLNDBN Body mass index quantitative trait locus 9
Reversed 0
HGVS NC_000020.10:g.54824336T>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000022657.4,