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rs121909615

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121909615(C;T)
Make rs121909615(T;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position154586390
GeneFGA
is asnp
is mentioned by
dbSNPrs121909615
ebirs121909615
HLIrs121909615
Exacrs121909615
Varsomers121909615
Maprs121909615
PheGenIrs121909615
hapmaprs121909615
1000 genomesrs121909615
hgdprs121909615
ensemblrs121909615
gopubmedrs121909615
geneviewrs121909615
scholarrs121909615
googlers121909615
pharmgkbrs121909615
gwascentralrs121909615
openSNPrs121909615
23andMers121909615
23andMe allrs121909615
SNP Nexus

SNPshotrs121909615
SNPdbers121909615
MSV3drs121909615
GWAS Ctlgrs121909615
Max Magnitude0
OMIM134820
Desc
Variant0024
Relatedalso
ClinVar
Risk rs121909615(T;T)
Alt rs121909615(T;T)
Reference rs121909615(C;C)
Significance Other
Disease FIBRINOGEN KEOKUK
Variation info
Gene FGA
CLNDBN FIBRINOGEN KEOKUK
Reversed 1
HGVS NC_000004.11:g.155507542G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000017880.2,