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rs267606789

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs267606789(C;T)
Make rs267606789(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position6151874
GeneF13A1
is asnp
is mentioned by
dbSNPrs267606789
ebirs267606789
HLIrs267606789
Exacrs267606789
Varsomers267606789
Maprs267606789
PheGenIrs267606789
hapmaprs267606789
1000 genomesrs267606789
hgdprs267606789
ensemblrs267606789
gopubmedrs267606789
geneviewrs267606789
scholarrs267606789
googlers267606789
pharmgkbrs267606789
gwascentralrs267606789
openSNPrs267606789
23andMers267606789
23andMe allrs267606789
SNP Nexus

SNPshotrs267606789
SNPdbers267606789
MSV3drs267606789
GWAS Ctlgrs267606789
Max Magnitude0
ClinVar
Risk rs267606789(T;T)
Alt rs267606789(T;T)
Reference rs267606789(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.6152107G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000018004.27,