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rs121913072

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121913072(A;A)
Make rs121913072(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position6222165
GeneF13A1
is asnp
is mentioned by
dbSNPrs121913072
ebirs121913072
HLIrs121913072
Exacrs121913072
Varsomers121913072
Maprs121913072
PheGenIrs121913072
hapmaprs121913072
1000 genomesrs121913072
hgdprs121913072
ensemblrs121913072
gopubmedrs121913072
geneviewrs121913072
scholarrs121913072
googlers121913072
pharmgkbrs121913072
gwascentralrs121913072
openSNPrs121913072
23andMers121913072
23andMe allrs121913072
SNP Nexus

SNPshotrs121913072
SNPdbers121913072
MSV3drs121913072
GWAS Ctlgrs121913072
Max Magnitude0
OMIM134570
Desc
Variant0011
Relatedalso
ClinVar
Risk rs121913072(A;A)
Alt rs121913072(A;A)
Reference rs121913072(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.6222398C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000017998.23,