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rs121913092

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs121913092(A;G)
Make rs121913092(G;G)
ReferenceGRCh38 38.1/141
Chromosome4
Position154606770
GeneFGG
is asnp
is mentioned by
dbSNPrs121913092
ebirs121913092
HLIrs121913092
Exacrs121913092
Varsomers121913092
Maprs121913092
PheGenIrs121913092
hapmaprs121913092
1000 genomesrs121913092
hgdprs121913092
ensemblrs121913092
gopubmedrs121913092
geneviewrs121913092
scholarrs121913092
googlers121913092
pharmgkbrs121913092
gwascentralrs121913092
openSNPrs121913092
23andMers121913092
23andMe allrs121913092
SNP Nexus

SNPshotrs121913092
SNPdbers121913092
MSV3drs121913092
GWAS Ctlgrs121913092
Max Magnitude0
OMIM134850
Desc
Variant0008
Relatedalso
ClinVar
Risk rs121913092(G;G)
Alt rs121913092(G;G)
Reference rs121913092(A;A)
Significance Other
Disease FIBRINOGEN NAGOYA 1
Variation info
Gene FGG
CLNDBN FIBRINOGEN NAGOYA 1
Reversed 1
HGVS NC_000004.11:g.155527922T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000017788.1,