Have questions? Visit https://www.reddit.com/r/SNPedia

rs121909613

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121909613(C;T)
Make rs121909613(T;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position154585712
GeneFGA
is asnp
is mentioned by
dbSNPrs121909613
ebirs121909613
HLIrs121909613
Exacrs121909613
Varsomers121909613
Maprs121909613
PheGenIrs121909613
hapmaprs121909613
1000 genomesrs121909613
hgdprs121909613
ensemblrs121909613
gopubmedrs121909613
geneviewrs121909613
scholarrs121909613
googlers121909613
pharmgkbrs121909613
gwascentralrs121909613
openSNPrs121909613
23andMers121909613
23andMe allrs121909613
SNP Nexus

SNPshotrs121909613
SNPdbers121909613
MSV3drs121909613
GWAS Ctlgrs121909613
Max Magnitude0
OMIM134820
Desc
Variant0014
Relatedalso
ClinVar
Risk rs121909613(A,G,T;A,G,T)
Alt rs121909613(A,G,T;A,G,T)
Reference rs121909613(C;C)
Significance Other
Disease FIBRINOGEN DUSART
Variation info
Gene FGA
CLNDBN FIBRINOGEN DUSART
Reversed 1
HGVS NC_000004.11:g.155506864G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000017872.5,