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rs121909614

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs121909614(A;A)
Make rs121909614(A;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position154589501
GeneFGA
is asnp
is mentioned by
dbSNPrs121909614
ebirs121909614
HLIrs121909614
Exacrs121909614
Varsomers121909614
Maprs121909614
PheGenIrs121909614
hapmaprs121909614
1000 genomesrs121909614
hgdprs121909614
ensemblrs121909614
gopubmedrs121909614
geneviewrs121909614
scholarrs121909614
googlers121909614
pharmgkbrs121909614
gwascentralrs121909614
openSNPrs121909614
23andMers121909614
23andMe allrs121909614
SNP Nexus

SNPshotrs121909614
SNPdbers121909614
MSV3drs121909614
GWAS Ctlgrs121909614
Max Magnitude0
OMIM134820
Desc
Variant0015
Relatedalso
ClinVar
Risk rs121909614(A;A)
Alt rs121909614(A;A)
Reference rs121909614(T;T)
Significance Other
Disease FIBRINOGEN CANTERBURY
Variation info
Gene FGA
CLNDBN FIBRINOGEN CANTERBURY
Reversed 1
HGVS NC_000004.11:g.155510653A>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000017874.2,