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rs6708166

From SNPedia

Orientationplus
Stabilizedplus
Make rs6708166(A;A)
Make rs6708166(A;G)
Make rs6708166(G;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position30303914
is asnp
is mentioned by
dbSNPrs6708166
dbSNP (classic)rs6708166
ClinGenrs6708166
ebirs6708166
HLIrs6708166
Exacrs6708166
Gnomadrs6708166
Varsomers6708166
LitVarrs6708166
Maprs6708166
PheGenIrs6708166
Biobankrs6708166
1000 genomesrs6708166
hgdprs6708166
ensemblrs6708166
geneviewrs6708166
scholarrs6708166
googlers6708166
pharmgkbrs6708166
gwascentralrs6708166
openSNPrs6708166
23andMers6708166
SNPshotrs6708166
SNPdbers6708166
MSV3drs6708166
GWAS Ctlgrs6708166
GMAF0.2415
Max Magnitude0
? (A;A) (A;G) (G;G) 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 A
P-val 0.000001
Odds Ratio 0.1700 [0.09-0.25] IU/dL decrease