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rs121913074

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs121913074(A;G)
Make rs121913074(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position6224808
GeneF13A1
is asnp
is mentioned by
dbSNPrs121913074
ebirs121913074
HLIrs121913074
Exacrs121913074
Varsomers121913074
Maprs121913074
PheGenIrs121913074
hapmaprs121913074
1000 genomesrs121913074
hgdprs121913074
ensemblrs121913074
gopubmedrs121913074
geneviewrs121913074
scholarrs121913074
googlers121913074
pharmgkbrs121913074
gwascentralrs121913074
openSNPrs121913074
23andMers121913074
23andMe allrs121913074
SNP Nexus

SNPshotrs121913074
SNPdbers121913074
MSV3drs121913074
GWAS Ctlgrs121913074
Max Magnitude0
OMIM134570
Desc
Variant0013
Relatedalso
ClinVar
Risk rs121913074(G;G)
Alt rs121913074(G;G)
Reference rs121913074(A;A)
Significance Pathogenic
Disease Factor xiii
Variation info
Gene F13A1
CLNDBN Factor xiii, a subunit, deficiency of
Reversed 1
HGVS NC_000006.11:g.6225041T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000018000.27,