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rs121909606

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121909606(C;T)
Make rs121909606(T;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position154589514
GeneFGA
is asnp
is mentioned by
dbSNPrs121909606
ebirs121909606
HLIrs121909606
Exacrs121909606
Varsomers121909606
Maprs121909606
PheGenIrs121909606
hapmaprs121909606
1000 genomesrs121909606
hgdprs121909606
ensemblrs121909606
gopubmedrs121909606
geneviewrs121909606
scholarrs121909606
googlers121909606
pharmgkbrs121909606
gwascentralrs121909606
openSNPrs121909606
23andMers121909606
23andMe allrs121909606
SNP Nexus

SNPshotrs121909606
SNPdbers121909606
MSV3drs121909606
GWAS Ctlgrs121909606
Max Magnitude0
OMIM134820
Desc
Variant0003
Relatedalso
ClinVar
Risk rs121909606(T;T)
Alt rs121909606(T;T)
Reference rs121909606(C;C)
Significance Pathogenic
Disease Dysfibrinogenemia
Variation info
Gene FGA
CLNDBN Dysfibrinogenemia
Reversed 1
HGVS NC_000004.11:g.155510666G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000017825.7,