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rs7025162

From SNPedia

Orientationplus
Stabilizedplus
Make rs7025162(C;C)
Make rs7025162(C;T)
Make rs7025162(T;T)
ReferenceGRCh38 38.1/142
Chromosome9
Position133290774
is asnp
is mentioned by
dbSNPrs7025162
ebirs7025162
HLIrs7025162
Exacrs7025162
Varsomers7025162
Maprs7025162
PheGenIrs7025162
hapmaprs7025162
1000 genomesrs7025162
hgdprs7025162
ensemblrs7025162
gopubmedrs7025162
geneviewrs7025162
scholarrs7025162
googlers7025162
pharmgkbrs7025162
gwascentralrs7025162
openSNPrs7025162
23andMers7025162
23andMe allrs7025162
SNP Nexus

SNPshotrs7025162
SNPdbers7025162
MSV3drs7025162
GWAS Ctlgrs7025162
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 24094242OA-icon.png]
Trait Serum alkaline phosphatase levels
Title Genome-wide association study on serum alkaline phosphatase levels in a Chinese population.
Risk Allele A
P-val 3E-27
Odds Ratio .05 [0.039-0.055] U/L decrease