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rs7306642

From SNPedia

Orientationplus
Stabilizedplus
Make rs7306642(A;A)
Make rs7306642(A;C)
Make rs7306642(C;C)
ReferenceGRCh38 38.1/141
Chromosome12
Position103745256
GeneSTAB2
is asnp
is mentioned by
dbSNPrs7306642
dbSNP (old)rs7306642
ClinGenrs7306642
ebirs7306642
HLIrs7306642
Exacrs7306642
Varsomers7306642
Maprs7306642
PheGenIrs7306642
Biobankrs7306642
1000 genomesrs7306642
hgdprs7306642
ensemblrs7306642
gopubmedrs7306642
geneviewrs7306642
scholarrs7306642
googlers7306642
pharmgkbrs7306642
gwascentralrs7306642
openSNPrs7306642
23andMers7306642
23andMe allrs7306642
SNP Nexus

SNPshotrs7306642
SNPdbers7306642
MSV3drs7306642
GWAS Ctlgrs7306642
GMAF0.0753
Max Magnitude
? (A;A) (A;C) (C;C) 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 0.000003
Odds Ratio 0.3000 [0.18-0.42] IU/dL increase


GET Evidence
STAB2-P2039T
aa_change Pro2039Thr
aa_change_short P2039T
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.104759
summary