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rs121909609

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121909609(C;T)
Make rs121909609(T;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position154589507
GeneFGA
is asnp
is mentioned by
dbSNPrs121909609
ebirs121909609
HLIrs121909609
Exacrs121909609
Varsomers121909609
Maprs121909609
PheGenIrs121909609
hapmaprs121909609
1000 genomesrs121909609
hgdprs121909609
ensemblrs121909609
gopubmedrs121909609
geneviewrs121909609
scholarrs121909609
googlers121909609
pharmgkbrs121909609
gwascentralrs121909609
openSNPrs121909609
23andMers121909609
23andMe allrs121909609
SNP Nexus

SNPshotrs121909609
SNPdbers121909609
MSV3drs121909609
GWAS Ctlgrs121909609
Max Magnitude0
OMIM134820
Desc
Variant0008
Relatedalso
ClinVar
Risk rs121909609(T;T)
Alt rs121909609(T;T)
Reference rs121909609(C;C)
Significance Other
Disease FIBRINOGEN KYOTO 2
Variation info
Gene FGA
CLNDBN FIBRINOGEN KYOTO 2
Reversed 1
HGVS NC_000004.11:g.155510659G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000017844.2,