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rs121909621

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs121909621(G;G)
Make rs121909621(G;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position154569703
GeneFGB
is asnp
is mentioned by
dbSNPrs121909621
ebirs121909621
HLIrs121909621
Exacrs121909621
Varsomers121909621
Maprs121909621
PheGenIrs121909621
hapmaprs121909621
1000 genomesrs121909621
hgdprs121909621
ensemblrs121909621
gopubmedrs121909621
geneviewrs121909621
scholarrs121909621
googlers121909621
pharmgkbrs121909621
gwascentralrs121909621
openSNPrs121909621
23andMers121909621
23andMe allrs121909621
SNP Nexus

SNPshotrs121909621
SNPdbers121909621
MSV3drs121909621
GWAS Ctlgrs121909621
Max Magnitude0
OMIM134830
Desc
Variant0009
Relatedalso
ClinVar
Risk rs121909621(G;G)
Alt rs121909621(G;G)
Reference rs121909621(T;T)
Significance Pathogenic
Disease Afibrinogenemia
Variation info
Gene FGB
CLNDBN Afibrinogenemia, congenital
Reversed 0
HGVS NC_000004.11:g.155490855T>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000017815.28,