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rs267606788

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs267606788(C;C)
Make rs267606788(C;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position6248382
GeneF13A1
is asnp
is mentioned by
dbSNPrs267606788
ebirs267606788
HLIrs267606788
Exacrs267606788
Varsomers267606788
Maprs267606788
PheGenIrs267606788
hapmaprs267606788
1000 genomesrs267606788
hgdprs267606788
ensemblrs267606788
gopubmedrs267606788
geneviewrs267606788
scholarrs267606788
googlers267606788
pharmgkbrs267606788
gwascentralrs267606788
openSNPrs267606788
23andMers267606788
23andMe allrs267606788
SNP Nexus

SNPshotrs267606788
SNPdbers267606788
MSV3drs267606788
GWAS Ctlgrs267606788
Max Magnitude0
ClinVar
Risk rs267606788(C;C)
Alt rs267606788(C;C)
Reference rs267606788(T;T)
Significance Pathogenic
Disease Factor xiii
Variation info
Gene F13A1
CLNDBN Factor xiii, a subunit, deficiency of
Reversed 1
HGVS NC_000006.11:g.6248615A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000018005.28,