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rs121909608

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs121909608(A;G)
Make rs121909608(G;G)
ReferenceGRCh38 38.1/141
Chromosome4
Position154589505
GeneFGA
is asnp
is mentioned by
dbSNPrs121909608
ebirs121909608
HLIrs121909608
Exacrs121909608
Varsomers121909608
Maprs121909608
PheGenIrs121909608
hapmaprs121909608
1000 genomesrs121909608
hgdprs121909608
ensemblrs121909608
gopubmedrs121909608
geneviewrs121909608
scholarrs121909608
googlers121909608
pharmgkbrs121909608
gwascentralrs121909608
openSNPrs121909608
23andMers121909608
23andMe allrs121909608
SNP Nexus

SNPshotrs121909608
SNPdbers121909608
MSV3drs121909608
GWAS Ctlgrs121909608
Max Magnitude0
OMIM134820
Desc
Variant0007
Relatedalso
ClinVar
Risk rs121909608(G;G)
Alt rs121909608(G;G)
Reference rs121909608(A;A)
Significance Other
Disease FIBRINOGEN AARHUS 1
Variation info
Gene FGA
CLNDBN FIBRINOGEN AARHUS 1
Reversed 1
HGVS NC_000004.11:g.155510657T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000017843.1,