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rs121909619

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121909619(C;T)
Make rs121909619(T;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position154565913
GeneFGB
is asnp
is mentioned by
dbSNPrs121909619
ebirs121909619
HLIrs121909619
Exacrs121909619
Varsomers121909619
Maprs121909619
PheGenIrs121909619
hapmaprs121909619
1000 genomesrs121909619
hgdprs121909619
ensemblrs121909619
gopubmedrs121909619
geneviewrs121909619
scholarrs121909619
googlers121909619
pharmgkbrs121909619
gwascentralrs121909619
openSNPrs121909619
23andMers121909619
23andMe allrs121909619
SNP Nexus

SNPshotrs121909619
SNPdbers121909619
MSV3drs121909619
GWAS Ctlgrs121909619
Max Magnitude0
OMIM134830
Desc
Variant0006
Relatedalso
ClinVar
Risk rs121909619(T;T)
Alt rs121909619(T;T)
Reference rs121909619(C;C)
Significance Other
Disease FIBRINOGEN NIJMEGEN
Variation info
Gene FGB
CLNDBN FIBRINOGEN NIJMEGEN
Reversed 0
HGVS NC_000004.11:g.155487065C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000119098.3,