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rs121909622

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121909622(A;A)
Make rs121909622(A;G)
ReferenceGRCh38 38.1/141
Chromosome4
Position154570463
GeneFGB
is asnp
is mentioned by
dbSNPrs121909622
ebirs121909622
HLIrs121909622
Exacrs121909622
Varsomers121909622
Maprs121909622
PheGenIrs121909622
hapmaprs121909622
1000 genomesrs121909622
hgdprs121909622
ensemblrs121909622
gopubmedrs121909622
geneviewrs121909622
scholarrs121909622
googlers121909622
pharmgkbrs121909622
gwascentralrs121909622
openSNPrs121909622
23andMers121909622
23andMe allrs121909622
SNP Nexus

SNPshotrs121909622
SNPdbers121909622
MSV3drs121909622
GWAS Ctlgrs121909622
Max Magnitude0
OMIM134830
Desc
Variant0010
Relatedalso
ClinVar
Risk rs121909622(A;A)
Alt rs121909622(A;A)
Reference rs121909622(G;G)
Significance Pathogenic
Disease Afibrinogenemia
Variation info
Gene FGB
CLNDBN Afibrinogenemia, congenital
Reversed 0
HGVS NC_000004.11:g.155491615G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000017816.28,