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rs121909625

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121909625(C;T)
Make rs121909625(T;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position154565832
GeneFGB
is asnp
is mentioned by
dbSNPrs121909625
ebirs121909625
HLIrs121909625
Exacrs121909625
Varsomers121909625
Maprs121909625
PheGenIrs121909625
hapmaprs121909625
1000 genomesrs121909625
hgdprs121909625
ensemblrs121909625
gopubmedrs121909625
geneviewrs121909625
scholarrs121909625
googlers121909625
pharmgkbrs121909625
gwascentralrs121909625
openSNPrs121909625
23andMers121909625
23andMe allrs121909625
SNP Nexus

SNPshotrs121909625
SNPdbers121909625
MSV3drs121909625
GWAS Ctlgrs121909625
Max Magnitude0
OMIM134830
Desc
Variant0016
Relatedalso
ClinVar
Risk rs121909625(T;T)
Alt rs121909625(T;T)
Reference rs121909625(C;C)
Significance Pathogenic
Disease Afibrinogenemia
Variation info
Gene FGB
CLNDBN Afibrinogenemia, congenital
Reversed 0
HGVS NC_000004.11:g.155486984C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000017822.30,