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rs121909605

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121909605(G;T)
Make rs121909605(T;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position154589525
GeneFGA
is asnp
is mentioned by
dbSNPrs121909605
ebirs121909605
HLIrs121909605
Exacrs121909605
Varsomers121909605
Maprs121909605
PheGenIrs121909605
hapmaprs121909605
1000 genomesrs121909605
hgdprs121909605
ensemblrs121909605
gopubmedrs121909605
geneviewrs121909605
scholarrs121909605
googlers121909605
pharmgkbrs121909605
gwascentralrs121909605
openSNPrs121909605
23andMers121909605
23andMe allrs121909605
SNP Nexus

SNPshotrs121909605
SNPdbers121909605
MSV3drs121909605
GWAS Ctlgrs121909605
Max Magnitude0
OMIM134820
Desc
Variant0002
Relatedalso
ClinVar
Risk rs121909605(T;T)
Alt rs121909605(T;T)
Reference rs121909605(G;G)
Significance Other
Disease FIBRINOGEN ROUEN 1
Variation info
Gene FGA
CLNDBN FIBRINOGEN ROUEN 1
Reversed 1
HGVS NC_000004.11:g.155510677C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000017824.1,