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rs3733403

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs3733403(C;G)
Make rs3733403(G;G)
ReferenceGRCh38 38.1/141
Chromosome4
Position186265981
GeneF11
is asnp
is mentioned by
dbSNPrs3733403
dbSNP (old)rs3733403
ClinGenrs3733403
ebirs3733403
HLIrs3733403
Exacrs3733403
Gnomadrs3733403
Varsomers3733403
Maprs3733403
PheGenIrs3733403
Biobankrs3733403
1000 genomesrs3733403
hgdprs3733403
ensemblrs3733403
gopubmedrs3733403
geneviewrs3733403
scholarrs3733403
googlers3733403
pharmgkbrs3733403
gwascentralrs3733403
openSNPrs3733403
23andMers3733403
23andMe allrs3733403
SNP Nexus

SNPshotrs3733403
SNPdbers3733403
MSV3drs3733403
GWAS Ctlgrs3733403
Max Magnitude0
? (C;C) (C;G) (G;G) 28
[PMID 24086496OA-icon.png] Genetic variants of coagulation factor XI show association with ischemic stroke up to 70 years of age


ClinVar
Risk rs3733403(G;G)
Alt rs3733403(G;G)
Reference Rs3733403(C;C)
Significance Non-pathogenic
Disease Hereditary factor XI deficiency disease
Variation info
Gene F11
CLNDBN Hereditary factor XI deficiency disease
Reversed 0
HGVS NC_000004.11:g.187187135C>G
CLNSRC
CLNACC RCV000294092.1,