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rs2225614

From SNPedia

Orientationminus
Stabilizedminus
Make rs2225614(G;G)
Make rs2225614(G;T)
Make rs2225614(T;T)
ReferenceGRCh38 38.1/141
Chromosome9
Position24111282
is asnp
is mentioned by
dbSNPrs2225614
ebirs2225614
HLIrs2225614
Exacrs2225614
Varsomers2225614
Maprs2225614
PheGenIrs2225614
hapmaprs2225614
1000 genomesrs2225614
hgdprs2225614
ensemblrs2225614
gopubmedrs2225614
geneviewrs2225614
scholarrs2225614
googlers2225614
pharmgkbrs2225614
gwascentralrs2225614
openSNPrs2225614
23andMers2225614
23andMe allrs2225614
SNP Nexus

SNPshotrs2225614
SNPdbers2225614
MSV3drs2225614
GWAS Ctlgrs2225614
GMAF0.3118
Max Magnitude
? (G;G) (G;T) (T;T) 28
GWAS snp
PMID [PMID 19197348OA-icon.png]
Trait Quantitative traits
Title Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae
Risk Allele C
P-val 0.000003
Odds Ratio 0.21 [NR] lb. decrease

Weight being the quantitative trait associated with in [PMID 19197348OA-icon.png]


GET Evidence
rs2225614
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.210938
summary