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rs10745527

From SNPedia

Orientationplus
Stabilizedplus
Make rs10745527(G;G)
Make rs10745527(G;T)
Make rs10745527(T;T)
ReferenceGRCh38 38.1/141
Chromosome12
Position90215240
is asnp
is mentioned by
dbSNPrs10745527
dbSNP (classic)rs10745527
ClinGenrs10745527
ebirs10745527
HLIrs10745527
Exacrs10745527
Gnomadrs10745527
Varsomers10745527
LitVarrs10745527
Maprs10745527
PheGenIrs10745527
Biobankrs10745527
1000 genomesrs10745527
hgdprs10745527
ensemblrs10745527
geneviewrs10745527
scholarrs10745527
googlers10745527
pharmgkbrs10745527
gwascentralrs10745527
openSNPrs10745527
23andMers10745527
SNPshotrs10745527
SNPdbers10745527
MSV3drs10745527
GWAS Ctlgrs10745527
GMAF0.3526
Max Magnitude0
? (G;G) (G;T) (T;T) 28


GWAS snp
PMID [PMID 21810271OA-icon.png]
Trait
Title Combined analysis of three genome-wide association studies on vWF and FVIII plasma levels.
Risk Allele G
P-val 0.000005
Odds Ratio 0.1600 [0.10-0.22] IU/dL increase