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rs121913096

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121913096(A;A)
Make rs121913096(A;G)
ReferenceGRCh38 38.1/141
Chromosome4
Position154606908
GeneFGG
is asnp
is mentioned by
dbSNPrs121913096
ebirs121913096
HLIrs121913096
Exacrs121913096
Varsomers121913096
Maprs121913096
PheGenIrs121913096
hapmaprs121913096
1000 genomesrs121913096
hgdprs121913096
ensemblrs121913096
gopubmedrs121913096
geneviewrs121913096
scholarrs121913096
googlers121913096
pharmgkbrs121913096
gwascentralrs121913096
openSNPrs121913096
23andMers121913096
23andMe allrs121913096
SNP Nexus

SNPshotrs121913096
SNPdbers121913096
MSV3drs121913096
GWAS Ctlgrs121913096
Max Magnitude0
OMIM134850
Desc
Variant0019
Relatedalso
ClinVar
Risk rs121913096(A;A)
Alt rs121913096(A;A)
Reference rs121913096(G;G)
Significance Other
Disease FIBRINOGEN HILLSBOROUGH
Variation info
Gene FGG
CLNDBN FIBRINOGEN HILLSBOROUGH
Reversed 1
HGVS NC_000004.11:g.155528060C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000017801.2,