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rs121909611

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs121909611(A;T)
Make rs121909611(T;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position154585991
GeneFGA
is asnp
is mentioned by
dbSNPrs121909611
ebirs121909611
HLIrs121909611
Exacrs121909611
Varsomers121909611
Maprs121909611
PheGenIrs121909611
hapmaprs121909611
1000 genomesrs121909611
hgdprs121909611
ensemblrs121909611
gopubmedrs121909611
geneviewrs121909611
scholarrs121909611
googlers121909611
pharmgkbrs121909611
gwascentralrs121909611
openSNPrs121909611
23andMers121909611
23andMe allrs121909611
SNP Nexus

SNPshotrs121909611
SNPdbers121909611
MSV3drs121909611
GWAS Ctlgrs121909611
Max Magnitude0
OMIM134820
Desc
Variant0011
Relatedalso
ClinVar
Risk rs121909611(T;T)
Alt rs121909611(T;T)
Reference rs121909611(A;A)
Significance Other
Disease FIBRINOGEN MARBURG
Variation info
Gene FGA
CLNDBN FIBRINOGEN MARBURG
Reversed 1
HGVS NC_000004.11:g.155507143T>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000017867.3,