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rs4525

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
(A;G)
(G;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position169542496
GeneF5
is asnp
is mentioned by
dbSNPrs4525
dbSNP (classic)rs4525
ClinGenrs4525
ebirs4525
HLIrs4525
Exacrs4525
Gnomadrs4525
Varsomers4525
LitVarrs4525
Maprs4525
PheGenIrs4525
Biobankrs4525
1000 genomesrs4525
hgdprs4525
ensemblrs4525
geneviewrs4525
scholarrs4525
googlers4525
pharmgkbrs4525
gwascentralrs4525
openSNPrs4525
23andMers4525
SNPshotrs4525
SNPdbers4525
MSV3drs4525
GWAS Ctlgrs4525
GMAF0.2438
Max Magnitude0
? (A;A) (A;G) (G;G) 28


[PMID 23690342OA-icon.png] Pharmacogenomic Association of Nonsynonymous SNPs in SIGLEC12, A1BG, and the Selectin Region and Cardiovascular Outcomes


ClinVar
Risk Rs4525(G;G)
Alt Rs4525(G;G)
Reference Rs4525(A;A)
Significance Probable-non-pathogenic
Disease not specified Budd-Chiari syndrome Thrombophilia due to activated protein C resistance Thrombophilia Factor V deficiency
Variation info
Gene F5
CLNDBN not specified Budd-Chiari syndrome Thrombophilia due to activated protein C resistance Thrombophilia Factor V deficiency
Reversed 1
HGVS NC_000001.10:g.169511734T>C
CLNSRC
CLNACC RCV000247612.1, RCV000290751.1, RCV000296476.1, RCV000350367.1, RCV000396448.1,