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rs121913075

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121913075(G;T)
Make rs121913075(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position197055720
GeneF13B
is asnp
is mentioned by
dbSNPrs121913075
ebirs121913075
HLIrs121913075
Exacrs121913075
Varsomers121913075
Maprs121913075
PheGenIrs121913075
hapmaprs121913075
1000 genomesrs121913075
hgdprs121913075
ensemblrs121913075
gopubmedrs121913075
geneviewrs121913075
scholarrs121913075
googlers121913075
pharmgkbrs121913075
gwascentralrs121913075
openSNPrs121913075
23andMers121913075
23andMe allrs121913075
SNP Nexus

SNPshotrs121913075
SNPdbers121913075
MSV3drs121913075
GWAS Ctlgrs121913075
Max Magnitude0
OMIM134580
Desc
Variant0002
Relatedalso
ClinVar
Risk rs121913075(T;T)
Alt rs121913075(T;T)
Reference rs121913075(G;G)
Significance Pathogenic
Disease Factor xiii
Variation info
Gene F13B
CLNDBN Factor xiii, b subunit, deficiency of
Reversed 1
HGVS NC_000001.10:g.197024850C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000017983.28,