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rs121913067

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121913067(A;A)
Make rs121913067(A;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position6305487
GeneF13A1
is asnp
is mentioned by
dbSNPrs121913067
ebirs121913067
HLIrs121913067
Exacrs121913067
Varsomers121913067
Maprs121913067
PheGenIrs121913067
hapmaprs121913067
1000 genomesrs121913067
hgdprs121913067
ensemblrs121913067
gopubmedrs121913067
geneviewrs121913067
scholarrs121913067
googlers121913067
pharmgkbrs121913067
gwascentralrs121913067
openSNPrs121913067
23andMers121913067
23andMe allrs121913067
SNP Nexus

SNPshotrs121913067
SNPdbers121913067
MSV3drs121913067
GWAS Ctlgrs121913067
Max Magnitude0
OMIM134570
Desc
Variant0005
Relatedalso
ClinVar
Risk rs121913067(A;A)
Alt rs121913067(A;A)
Reference rs121913067(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.6305720G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000017991.28,