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rs6110577

From SNPedia

Orientationplus
Stabilizedplus
Make rs6110577(C;C)
Make rs6110577(C;T)
Make rs6110577(T;T)
ReferenceGRCh38 38.1/141
Chromosome20
Position15355108
GeneMACROD2
is asnp
is mentioned by
dbSNPrs6110577
ebirs6110577
HLIrs6110577
Exacrs6110577
Varsomers6110577
Maprs6110577
PheGenIrs6110577
hapmaprs6110577
1000 genomesrs6110577
hgdprs6110577
ensemblrs6110577
gopubmedrs6110577
geneviewrs6110577
scholarrs6110577
googlers6110577
pharmgkbrs6110577
gwascentralrs6110577
openSNPrs6110577
23andMers6110577
23andMe allrs6110577
SNP Nexus

SNPshotrs6110577
SNPdbers6110577
MSV3drs6110577
GWAS Ctlgrs6110577
GMAF0.2837
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 19553259OA-icon.png]
Trait Obesity (extreme)
Title Common BMI-associated variants confer risk of extreme obesity
Risk Allele C
P-val 0.000005
Odds Ratio 1.40 [1.21-1.61]


GET Evidence
rs6110577
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.28125
summary