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rs267606787

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs267606787(C;T)
Make rs267606787(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position6145708
GeneF13A1
is asnp
is mentioned by
dbSNPrs267606787
ebirs267606787
HLIrs267606787
Exacrs267606787
Varsomers267606787
Maprs267606787
PheGenIrs267606787
hapmaprs267606787
1000 genomesrs267606787
hgdprs267606787
ensemblrs267606787
gopubmedrs267606787
geneviewrs267606787
scholarrs267606787
googlers267606787
pharmgkbrs267606787
gwascentralrs267606787
openSNPrs267606787
23andMers267606787
23andMe allrs267606787
SNP Nexus

SNPshotrs267606787
SNPdbers267606787
MSV3drs267606787
GWAS Ctlgrs267606787
Max Magnitude0
ClinVar
Risk rs267606787(T;T)
Alt rs267606787(T;T)
Reference rs267606787(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.6145941G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000018003.28,