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rs10125157

From SNPedia

Orientationplus
Stabilizedplus
Make rs10125157(A;A)
Make rs10125157(A;C)
Make rs10125157(C;C)
ReferenceGRCh38.p2 38.2/144
Chromosome9
Position118580943
is asnp
is mentioned by
dbSNPrs10125157
ebirs10125157
HLIrs10125157
Exacrs10125157
Varsomers10125157
Maprs10125157
PheGenIrs10125157
hapmaprs10125157
1000 genomesrs10125157
hgdprs10125157
ensemblrs10125157
gopubmedrs10125157
geneviewrs10125157
scholarrs10125157
googlers10125157
pharmgkbrs10125157
gwascentralrs10125157
openSNPrs10125157
23andMers10125157
23andMe allrs10125157
SNP Nexus

SNPshotrs10125157
SNPdbers10125157
MSV3drs10125157
GWAS Ctlgrs10125157
Max Magnitude
? (A;A) (A;C) (C;C) 28

[PMID 26083723] Lack of association between arterial stiffness and genetic variants by genome-wide association scan