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rs121913091

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs121913091(C;C)
Make rs121913091(C;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position154606827
GeneFGG
is asnp
is mentioned by
dbSNPrs121913091
ebirs121913091
HLIrs121913091
Exacrs121913091
Varsomers121913091
Maprs121913091
PheGenIrs121913091
hapmaprs121913091
1000 genomesrs121913091
hgdprs121913091
ensemblrs121913091
gopubmedrs121913091
geneviewrs121913091
scholarrs121913091
googlers121913091
pharmgkbrs121913091
gwascentralrs121913091
openSNPrs121913091
23andMers121913091
23andMe allrs121913091
SNP Nexus

SNPshotrs121913091
SNPdbers121913091
MSV3drs121913091
GWAS Ctlgrs121913091
Max Magnitude0
OMIM134850
Desc
Variant0006
Relatedalso
ClinVar
Risk rs121913091(C;C)
Alt rs121913091(C;C)
Reference rs121913091(T;T)
Significance Other
Disease FIBRINOGEN ASAHI
Variation info
Gene FGG
CLNDBN FIBRINOGEN ASAHI
Reversed 1
HGVS NC_000004.11:g.155527979A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000017786.2,