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rs387906287

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs387906287(A;A)
Make rs387906287(A;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position46907809
GeneMCFD2
is asnp
is mentioned by
dbSNPrs387906287
ebirs387906287
HLIrs387906287
Exacrs387906287
Varsomers387906287
Maprs387906287
PheGenIrs387906287
hapmaprs387906287
1000 genomesrs387906287
hgdprs387906287
ensemblrs387906287
gopubmedrs387906287
geneviewrs387906287
scholarrs387906287
googlers387906287
pharmgkbrs387906287
gwascentralrs387906287
openSNPrs387906287
23andMers387906287
23andMe allrs387906287
SNP Nexus

SNPshotrs387906287
SNPdbers387906287
MSV3drs387906287
GWAS Ctlgrs387906287
Max Magnitude0
ClinVar
Risk rs387906287(A;A)
Alt rs387906287(A;A)
Reference rs387906287(G;G)
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.47134948C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000003000.2,