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rs137852914

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs137852914(C;C)
Make rs137852914(C;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position46905497
GeneMCFD2
is asnp
is mentioned by
dbSNPrs137852914
ebirs137852914
HLIrs137852914
Exacrs137852914
Varsomers137852914
Maprs137852914
PheGenIrs137852914
hapmaprs137852914
1000 genomesrs137852914
hgdprs137852914
ensemblrs137852914
gopubmedrs137852914
geneviewrs137852914
scholarrs137852914
googlers137852914
pharmgkbrs137852914
gwascentralrs137852914
openSNPrs137852914
23andMers137852914
23andMe allrs137852914
SNP Nexus

SNPshotrs137852914
SNPdbers137852914
MSV3drs137852914
GWAS Ctlgrs137852914
Max Magnitude0
OMIM607788
Desc
Variant0007
Relatedalso
ClinVar
Risk rs137852914(C;C)
Alt rs137852914(C;C)
Reference rs137852914(T;T)
Significance Pathogenic
Disease Factor v and factor viii
Variation info
Gene MCFD2
CLNDBN Factor v and factor viii, combined deficiency of, 2
Reversed 1
HGVS NC_000002.11:g.47132636A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000003005.2,