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rs387906507

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs387906507(C;C)
Make rs387906507(C;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position113105879
GeneF7
is asnp
is mentioned by
dbSNPrs387906507
ebirs387906507
HLIrs387906507
Exacrs387906507
Varsomers387906507
Maprs387906507
PheGenIrs387906507
hapmaprs387906507
1000 genomesrs387906507
hgdprs387906507
ensemblrs387906507
gopubmedrs387906507
geneviewrs387906507
scholarrs387906507
googlers387906507
pharmgkbrs387906507
gwascentralrs387906507
openSNPrs387906507
23andMers387906507
23andMe allrs387906507
SNP Nexus

SNPshotrs387906507
SNPdbers387906507
MSV3drs387906507
GWAS Ctlgrs387906507
Max Magnitude0
ClinVar
Risk rs387906507(C;C)
Alt rs387906507(C;C)
Reference rs387906507(T;T)
Significance Pathogenic
Disease Factor VII deficiency
Variation info
Gene F7
CLNDBN Factor VII deficiency
Reversed 0
HGVS NC_000013.10:g.113760193T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000012856.3,