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rs121913071

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121913071(A;A)
Make rs121913071(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position6248328
GeneF13A1
is asnp
is mentioned by
dbSNPrs121913071
ebirs121913071
HLIrs121913071
Exacrs121913071
Varsomers121913071
Maprs121913071
PheGenIrs121913071
hapmaprs121913071
1000 genomesrs121913071
hgdprs121913071
ensemblrs121913071
gopubmedrs121913071
geneviewrs121913071
scholarrs121913071
googlers121913071
pharmgkbrs121913071
gwascentralrs121913071
openSNPrs121913071
23andMers121913071
23andMe allrs121913071
SNP Nexus

SNPshotrs121913071
SNPdbers121913071
MSV3drs121913071
GWAS Ctlgrs121913071
Max Magnitude0
OMIM134570
Desc
Variant0009
Relatedalso
ClinVar
Risk rs121913071(A;A)
Alt rs121913071(A;A)
Reference rs121913071(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.6248561C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000017995.27,