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rs121913069

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121913069(A;A)
Make rs121913069(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position6174640
GeneF13A1
is asnp
is mentioned by
dbSNPrs121913069
ebirs121913069
HLIrs121913069
Exacrs121913069
Varsomers121913069
Maprs121913069
PheGenIrs121913069
hapmaprs121913069
1000 genomesrs121913069
hgdprs121913069
ensemblrs121913069
gopubmedrs121913069
geneviewrs121913069
scholarrs121913069
googlers121913069
pharmgkbrs121913069
gwascentralrs121913069
openSNPrs121913069
23andMers121913069
23andMe allrs121913069
SNP Nexus

SNPshotrs121913069
SNPdbers121913069
MSV3drs121913069
GWAS Ctlgrs121913069
Max Magnitude0
OMIM134570
Desc
Variant0007
Relatedalso
ClinVar
Risk rs121913069(A;A)
Alt rs121913069(A;A)
Reference rs121913069(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.6174873C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000017993.27,