Have questions? Visit https://www.reddit.com/r/SNPedia

rs387906286

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs387906286(A;A)
Make rs387906286(A;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position46909018
GeneMCFD2
is asnp
is mentioned by
dbSNPrs387906286
ebirs387906286
HLIrs387906286
Exacrs387906286
Varsomers387906286
Maprs387906286
PheGenIrs387906286
hapmaprs387906286
1000 genomesrs387906286
hgdprs387906286
ensemblrs387906286
gopubmedrs387906286
geneviewrs387906286
scholarrs387906286
googlers387906286
pharmgkbrs387906286
gwascentralrs387906286
openSNPrs387906286
23andMers387906286
23andMe allrs387906286
SNP Nexus

SNPshotrs387906286
SNPdbers387906286
MSV3drs387906286
GWAS Ctlgrs387906286
Max Magnitude0
ClinVar
Risk rs387906286(A;A)
Alt rs387906286(A;A)
Reference rs387906286(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.47136157C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000002999.2,