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rs387906508

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs387906508(C;C)
Make rs387906508(C;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position113118590
GeneF7
is asnp
is mentioned by
dbSNPrs387906508
ebirs387906508
HLIrs387906508
Exacrs387906508
Varsomers387906508
Maprs387906508
PheGenIrs387906508
hapmaprs387906508
1000 genomesrs387906508
hgdprs387906508
ensemblrs387906508
gopubmedrs387906508
geneviewrs387906508
scholarrs387906508
googlers387906508
pharmgkbrs387906508
gwascentralrs387906508
openSNPrs387906508
23andMers387906508
23andMe allrs387906508
SNP Nexus

SNPshotrs387906508
SNPdbers387906508
MSV3drs387906508
GWAS Ctlgrs387906508
Max Magnitude0
ClinVar
Risk rs387906508(C;C)
Alt rs387906508(C;C)
Reference rs387906508(T;T)
Significance Pathogenic
Disease Factor VII deficiency
Variation info
Gene F7
CLNDBN Factor VII deficiency
Reversed 0
HGVS NC_000013.10:g.113772904T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000012871.3,