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rs121913094

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs121913094(A;T)
Make rs121913094(T;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position154606767
GeneFGG
is asnp
is mentioned by
dbSNPrs121913094
ebirs121913094
HLIrs121913094
Exacrs121913094
Varsomers121913094
Maprs121913094
PheGenIrs121913094
hapmaprs121913094
1000 genomesrs121913094
hgdprs121913094
ensemblrs121913094
gopubmedrs121913094
geneviewrs121913094
scholarrs121913094
googlers121913094
pharmgkbrs121913094
gwascentralrs121913094
openSNPrs121913094
23andMers121913094
23andMe allrs121913094
SNP Nexus

SNPshotrs121913094
SNPdbers121913094
MSV3drs121913094
GWAS Ctlgrs121913094
Max Magnitude0
OMIM134850
Desc
Variant0010
Relatedalso
ClinVar
Risk rs121913094(T;T)
Alt rs121913094(T;T)
Reference rs121913094(A;A)
Significance Other
Disease FIBRINOGEN MILANO 1
Variation info
Gene FGG
CLNDBN FIBRINOGEN MILANO 1
Reversed 1
HGVS NC_000004.11:g.155527919T>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000017790.5,