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rs121909604

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121909604(A;A)
Make rs121909604(A;G)
ReferenceGRCh38 38.1/141
Chromosome4
Position154589541
GeneFGA
is asnp
is mentioned by
dbSNPrs121909604
ebirs121909604
HLIrs121909604
Exacrs121909604
Varsomers121909604
Maprs121909604
PheGenIrs121909604
hapmaprs121909604
1000 genomesrs121909604
hgdprs121909604
ensemblrs121909604
gopubmedrs121909604
geneviewrs121909604
scholarrs121909604
googlers121909604
pharmgkbrs121909604
gwascentralrs121909604
openSNPrs121909604
23andMers121909604
23andMe allrs121909604
SNP Nexus

SNPshotrs121909604
SNPdbers121909604
MSV3drs121909604
GWAS Ctlgrs121909604
Max Magnitude0
OMIM134820
Desc
Variant0001
Relatedalso
ClinVar
Risk rs121909604(A;A)
Alt rs121909604(A;A)
Reference rs121909604(G;G)
Significance Other
Disease FIBRINOGEN LILLE 1
Variation info
Gene FGA
CLNDBN FIBRINOGEN LILLE 1
Reversed 1
HGVS NC_000004.11:g.155510693C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000017823.1,