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rs121913065

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121913065(C;T)
Make rs121913065(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position6266615
GeneF13A1
is asnp
is mentioned by
dbSNPrs121913065
ebirs121913065
HLIrs121913065
Exacrs121913065
Varsomers121913065
Maprs121913065
PheGenIrs121913065
hapmaprs121913065
1000 genomesrs121913065
hgdprs121913065
ensemblrs121913065
gopubmedrs121913065
geneviewrs121913065
scholarrs121913065
googlers121913065
pharmgkbrs121913065
gwascentralrs121913065
openSNPrs121913065
23andMers121913065
23andMe allrs121913065
SNP Nexus

SNPshotrs121913065
SNPdbers121913065
MSV3drs121913065
GWAS Ctlgrs121913065
Max Magnitude0
OMIM134570
Desc
Variant0003
Relatedalso
ClinVar
Risk rs121913065(T;T)
Alt rs121913065(T;T)
Reference rs121913065(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.6266848G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000017989.27,