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rs11906160

From SNPedia

Orientationplus
Stabilizedplus
Make rs11906160(A;A)
Make rs11906160(A;G)
Make rs11906160(G;G)
ReferenceGRCh38 38.1/141
Chromosome20
Position34977952
GeneMYH7B
is asnp
is mentioned by
dbSNPrs11906160
ebirs11906160
HLIrs11906160
Exacrs11906160
Varsomers11906160
Maprs11906160
PheGenIrs11906160
hapmaprs11906160
1000 genomesrs11906160
hgdprs11906160
ensemblrs11906160
gopubmedrs11906160
geneviewrs11906160
scholarrs11906160
googlers11906160
pharmgkbrs11906160
gwascentralrs11906160
openSNPrs11906160
23andMers11906160
23andMe allrs11906160
SNP Nexus

SNPshotrs11906160
SNPdbers11906160
MSV3drs11906160
GWAS Ctlgrs11906160
GMAF0.1423
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 22216198OA-icon.png]
Trait
Title A genome-wide association study of the Protein C anticoagulant pathway.
Risk Allele
P-val 0.000001
Odds Ratio None None


GET Evidence
MYH7B-A25T
aa_change Ala25Thr
aa_change_short A25T
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.155595
summary