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rs121913073

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121913073(G;T)
Make rs121913073(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position6224710
GeneF13A1
is asnp
is mentioned by
dbSNPrs121913073
ebirs121913073
HLIrs121913073
Exacrs121913073
Varsomers121913073
Maprs121913073
PheGenIrs121913073
hapmaprs121913073
1000 genomesrs121913073
hgdprs121913073
ensemblrs121913073
gopubmedrs121913073
geneviewrs121913073
scholarrs121913073
googlers121913073
pharmgkbrs121913073
gwascentralrs121913073
openSNPrs121913073
23andMers121913073
23andMe allrs121913073
SNP Nexus

SNPshotrs121913073
SNPdbers121913073
MSV3drs121913073
GWAS Ctlgrs121913073
Max Magnitude0
OMIM134570
Desc
Variant0012
Relatedalso
ClinVar
Risk rs121913073(T;T)
Alt rs121913073(T;T)
Reference rs121913073(G;G)
Significance Pathogenic
Disease Factor xiii
Variation info
Gene F13A1
CLNDBN Factor xiii, a subunit, deficiency of
Reversed 1
HGVS NC_000006.11:g.6224943C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000017999.28,