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rs121913066

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121913066(A;A)
Make rs121913066(A;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position6182121
GeneF13A1
is asnp
is mentioned by
dbSNPrs121913066
ebirs121913066
HLIrs121913066
Exacrs121913066
Varsomers121913066
Maprs121913066
PheGenIrs121913066
hapmaprs121913066
1000 genomesrs121913066
hgdprs121913066
ensemblrs121913066
gopubmedrs121913066
geneviewrs121913066
scholarrs121913066
googlers121913066
pharmgkbrs121913066
gwascentralrs121913066
openSNPrs121913066
23andMers121913066
23andMe allrs121913066
SNP Nexus

SNPshotrs121913066
SNPdbers121913066
MSV3drs121913066
GWAS Ctlgrs121913066
Max Magnitude0
OMIM134570
Desc
Variant0004
Relatedalso
ClinVar
Risk rs121913066(A,T;A,T)
Alt rs121913066(A,T;A,T)
Reference rs121913066(C;C)
Significance Pathogenic
Disease Factor xiii
Variation info
Gene F13A1
CLNDBN Factor xiii, a subunit, deficiency of
Reversed 1
HGVS NC_000006.11:g.6182354G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000017990.24,