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rs121913095

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121913095(C;C)
Make rs121913095(C;G)
ReferenceGRCh38 38.1/141
Chromosome4
Position154605028
GeneFGG
is asnp
is mentioned by
dbSNPrs121913095
ebirs121913095
HLIrs121913095
Exacrs121913095
Varsomers121913095
Maprs121913095
PheGenIrs121913095
hapmaprs121913095
1000 genomesrs121913095
hgdprs121913095
ensemblrs121913095
gopubmedrs121913095
geneviewrs121913095
scholarrs121913095
googlers121913095
pharmgkbrs121913095
gwascentralrs121913095
openSNPrs121913095
23andMers121913095
23andMe allrs121913095
SNP Nexus

SNPshotrs121913095
SNPdbers121913095
MSV3drs121913095
GWAS Ctlgrs121913095
Max Magnitude0
OMIM134850
Desc
Variant0014
Relatedalso
ClinVar
Risk rs121913095(C;C)
Alt rs121913095(C;C)
Reference rs121913095(G;G)
Significance Other
Disease FIBRINOGEN MATSUMOTO 1
Variation info
Gene FGG
CLNDBN FIBRINOGEN MATSUMOTO 1
Reversed 1
HGVS NC_000004.11:g.155526180C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000017796.2,