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rs2815822

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs2815822(G;G)
Make rs2815822(G;T)
ReferenceGRCh38 38.1/142
Chromosome6
Position6320575
GeneF13A1
is asnp
is mentioned by
dbSNPrs2815822
ebirs2815822
HLIrs2815822
Exacrs2815822
Varsomers2815822
Maprs2815822
PheGenIrs2815822
hapmaprs2815822
1000 genomesrs2815822
hgdprs2815822
ensemblrs2815822
gopubmedrs2815822
geneviewrs2815822
scholarrs2815822
googlers2815822
pharmgkbrs2815822
gwascentralrs2815822
openSNPrs2815822
23andMers2815822
23andMe allrs2815822
SNP Nexus

SNPshotrs2815822
SNPdbers2815822
MSV3drs2815822
GWAS Ctlgrs2815822
Max Magnitude0
? (G;G) (G;T) (T;T) 28
ClinVar
Risk rs2815822(G;G)
Alt rs2815822(G;G)
Reference rs2815822(T;T)
Significance Pathogenic
Disease Factor xiii
Variation info
Gene F13A1
CLNDBN Factor xiii, a subunit, deficiency of
Reversed 0
HGVS NC_000006.11:g.6320808T\x3d
CLNSRC OMIM Allelic Variant
CLNACC RCV000022542.27,