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rs121913068

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121913068(A;A)
Make rs121913068(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position6174823
GeneF13A1
is asnp
is mentioned by
dbSNPrs121913068
ebirs121913068
HLIrs121913068
Exacrs121913068
Varsomers121913068
Maprs121913068
PheGenIrs121913068
hapmaprs121913068
1000 genomesrs121913068
hgdprs121913068
ensemblrs121913068
gopubmedrs121913068
geneviewrs121913068
scholarrs121913068
googlers121913068
pharmgkbrs121913068
gwascentralrs121913068
openSNPrs121913068
23andMers121913068
23andMe allrs121913068
SNP Nexus

SNPshotrs121913068
SNPdbers121913068
MSV3drs121913068
GWAS Ctlgrs121913068
Max Magnitude0
OMIM134570
Desc
Variant0006
Relatedalso
ClinVar
Risk rs121913068(A;A)
Alt rs121913068(A;A)
Reference rs121913068(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.6175056C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000017992.28,