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rs797044453

From SNPedia

Orientationminus
Make rs797044453(-;-)
Make rs797044453(-;G)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position197052691
GeneF13B
is asnp
is mentioned by
dbSNPrs797044453
ebirs797044453
HLIrs797044453
Exacrs797044453
Varsomers797044453
Maprs797044453
PheGenIrs797044453
hapmaprs797044453
1000 genomesrs797044453
hgdprs797044453
ensemblrs797044453
gopubmedrs797044453
geneviewrs797044453
scholarrs797044453
googlers797044453
pharmgkbrs797044453
gwascentralrs797044453
openSNPrs797044453
23andMers797044453
23andMe allrs797044453
SNP Nexus

SNPshotrs797044453
SNPdbers797044453
MSV3drs797044453
GWAS Ctlgrs797044453
Max Magnitude
ClinVar
Risk rs797044453(;)
Alt rs797044453(;)
Reference rs797044453(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.197021821delC
CLNSRC OMIM Allelic Variant
CLNACC RCV000017986.30,