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rs121913090

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs121913090(A;T)
Make rs121913090(T;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position154606833
GeneFGG
is asnp
is mentioned by
dbSNPrs121913090
ebirs121913090
HLIrs121913090
Exacrs121913090
Varsomers121913090
Maprs121913090
PheGenIrs121913090
hapmaprs121913090
1000 genomesrs121913090
hgdprs121913090
ensemblrs121913090
gopubmedrs121913090
geneviewrs121913090
scholarrs121913090
googlers121913090
pharmgkbrs121913090
gwascentralrs121913090
openSNPrs121913090
23andMers121913090
23andMe allrs121913090
SNP Nexus

SNPshotrs121913090
SNPdbers121913090
MSV3drs121913090
GWAS Ctlgrs121913090
GMAF0.0004591
Max Magnitude0
OMIM134850
Desc
Variant0005
Relatedalso
ClinVar
Risk rs121913090(T;T)
Alt rs121913090(T;T)
Reference rs121913090(A;A)
Significance Other
Disease FIBRINOGEN BALTIMORE 3
Variation info
Gene FGG
CLNDBN FIBRINOGEN BALTIMORE 3
Reversed 1
HGVS NC_000004.11:g.155527985T>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000017785.2,