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rs121909610

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121909610(A;A)
Make rs121909610(A;G)
ReferenceGRCh38 38.1/141
Chromosome4
Position154586071
GeneFGA
is asnp
is mentioned by
dbSNPrs121909610
ebirs121909610
HLIrs121909610
Exacrs121909610
Varsomers121909610
Maprs121909610
PheGenIrs121909610
hapmaprs121909610
1000 genomesrs121909610
hgdprs121909610
ensemblrs121909610
gopubmedrs121909610
geneviewrs121909610
scholarrs121909610
googlers121909610
pharmgkbrs121909610
gwascentralrs121909610
openSNPrs121909610
23andMers121909610
23andMe allrs121909610
SNP Nexus

SNPshotrs121909610
SNPdbers121909610
MSV3drs121909610
GWAS Ctlgrs121909610
Max Magnitude0
OMIM134820
Desc
Variant0009
Relatedalso
ClinVar
Risk rs121909610(A;A)
Alt rs121909610(A;A)
Reference rs121909610(G;G)
Significance Other
Disease FIBRINOGEN CARACAS 2
Variation info
Gene FGA
CLNDBN FIBRINOGEN CARACAS 2
Reversed 1
HGVS NC_000004.11:g.155507223C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000017865.3,