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rs121909616

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121909616(C;T)
Make rs121909616(T;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position154565823
GeneFGB
is asnp
is mentioned by
dbSNPrs121909616
ebirs121909616
HLIrs121909616
Exacrs121909616
Varsomers121909616
Maprs121909616
PheGenIrs121909616
hapmaprs121909616
1000 genomesrs121909616
hgdprs121909616
ensemblrs121909616
gopubmedrs121909616
geneviewrs121909616
scholarrs121909616
googlers121909616
pharmgkbrs121909616
gwascentralrs121909616
openSNPrs121909616
23andMers121909616
23andMe allrs121909616
SNP Nexus

SNPshotrs121909616
SNPdbers121909616
MSV3drs121909616
GWAS Ctlgrs121909616
Max Magnitude0
OMIM134830
Desc
Variant0002
Relatedalso
OMIM134830
Desc
Variant0006
Relatedalso
ClinVar
Risk rs121909616(T;T)
Alt rs121909616(T;T)
Reference rs121909616(C;C)
Significance Other
Disease FIBRINOGEN CHRISTCHURCH 2
Variation info
Gene FGB
CLNDBN FIBRINOGEN CHRISTCHURCH 2
Reversed 0
HGVS NC_000004.11:g.155486975C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000017804.5,