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rs121913070

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121913070(G;T)
Make rs121913070(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position6195859
GeneF13A1
is asnp
is mentioned by
dbSNPrs121913070
ebirs121913070
HLIrs121913070
Exacrs121913070
Varsomers121913070
Maprs121913070
PheGenIrs121913070
hapmaprs121913070
1000 genomesrs121913070
hgdprs121913070
ensemblrs121913070
gopubmedrs121913070
geneviewrs121913070
scholarrs121913070
googlers121913070
pharmgkbrs121913070
gwascentralrs121913070
openSNPrs121913070
23andMers121913070
23andMe allrs121913070
SNP Nexus

SNPshotrs121913070
SNPdbers121913070
MSV3drs121913070
GWAS Ctlgrs121913070
Max Magnitude0
OMIM134570
Desc
Variant0008
Relatedalso
ClinVar
Risk rs121913070(T;T)
Alt rs121913070(T;T)
Reference rs121913070(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.6196092C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000017994.23,