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rs10783050

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in complete genomics
Make rs10783050(C;C)
Make rs10783050(C;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position96571527
is asnp
is mentioned by
dbSNPrs10783050
ebirs10783050
HLIrs10783050
Exacrs10783050
Varsomers10783050
Maprs10783050
PheGenIrs10783050
hapmaprs10783050
1000 genomesrs10783050
hgdprs10783050
ensemblrs10783050
gopubmedrs10783050
geneviewrs10783050
scholarrs10783050
googlers10783050
pharmgkbrs10783050
gwascentralrs10783050
openSNPrs10783050
23andMers10783050
23andMe allrs10783050
SNP Nexus

SNPshotrs10783050
SNPdbers10783050
MSV3drs10783050
GWAS Ctlgrs10783050
GMAF0.3223
Max Magnitude0
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 19079260]
Trait Body mass index
Title Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity
Risk Allele C
P-val 0.000004
Odds Ratio 2.60 [1.50-3.70] % SD



GET Evidence
rs10783050
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.28125
summary