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rs121909623

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121909623(C;T)
Make rs121909623(T;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position154567688
GeneFGB
is asnp
is mentioned by
dbSNPrs121909623
ebirs121909623
HLIrs121909623
Exacrs121909623
Varsomers121909623
Maprs121909623
PheGenIrs121909623
hapmaprs121909623
1000 genomesrs121909623
hgdprs121909623
ensemblrs121909623
gopubmedrs121909623
geneviewrs121909623
scholarrs121909623
googlers121909623
pharmgkbrs121909623
gwascentralrs121909623
openSNPrs121909623
23andMers121909623
23andMe allrs121909623
SNP Nexus

SNPshotrs121909623
SNPdbers121909623
MSV3drs121909623
GWAS Ctlgrs121909623
Max Magnitude0
OMIM134830
Desc
Variant0011
Relatedalso
ClinVar
Risk rs121909623(T;T)
Alt rs121909623(T;T)
Reference rs121909623(C;C)
Significance Other
Disease FIBRINOGEN LONGMONT
Variation info
Gene FGB
CLNDBN FIBRINOGEN LONGMONT
Reversed 0
HGVS NC_000004.11:g.155488840C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000017817.1,