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rs121913064

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121913064(A;A)
Make rs121913064(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position6151813
GeneF13A1
is asnp
is mentioned by
dbSNPrs121913064
ebirs121913064
HLIrs121913064
Exacrs121913064
Varsomers121913064
Maprs121913064
PheGenIrs121913064
hapmaprs121913064
1000 genomesrs121913064
hgdprs121913064
ensemblrs121913064
gopubmedrs121913064
geneviewrs121913064
scholarrs121913064
googlers121913064
pharmgkbrs121913064
gwascentralrs121913064
openSNPrs121913064
23andMers121913064
23andMe allrs121913064
SNP Nexus

SNPshotrs121913064
SNPdbers121913064
MSV3drs121913064
GWAS Ctlgrs121913064
Max Magnitude0
OMIM134570
Desc
Variant0002
Relatedalso
ClinVar
Risk rs121913064(A,T;A,T)
Alt rs121913064(A,T;A,T)
Reference rs121913064(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.6152046C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000017988.27,