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rs121909624

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs121909624(A;A)
Make rs121909624(A;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position154567707
GeneFGB
is asnp
is mentioned by
dbSNPrs121909624
ebirs121909624
HLIrs121909624
Exacrs121909624
Varsomers121909624
Maprs121909624
PheGenIrs121909624
hapmaprs121909624
1000 genomesrs121909624
hgdprs121909624
ensemblrs121909624
gopubmedrs121909624
geneviewrs121909624
scholarrs121909624
googlers121909624
pharmgkbrs121909624
gwascentralrs121909624
openSNPrs121909624
23andMers121909624
23andMe allrs121909624
SNP Nexus

SNPshotrs121909624
SNPdbers121909624
MSV3drs121909624
GWAS Ctlgrs121909624
Max Magnitude0
OMIM134830
Desc
Variant0015
Relatedalso
ClinVar
Risk rs121909624(A;A)
Alt rs121909624(A;A)
Reference rs121909624(T;T)
Significance Pathogenic
Disease Afibrinogenemia
Variation info
Gene FGB
CLNDBN Afibrinogenemia, congenital
Reversed 0
HGVS NC_000004.11:g.155488859T>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000017821.25,