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rs387906506

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs387906506(-;-)
Make rs387906506(-;C)
ReferenceGRCh38 38.1/141
Chromosome13
Position113147444
GeneF10
is asnp
is mentioned by
dbSNPrs387906506
ebirs387906506
HLIrs387906506
Exacrs387906506
Varsomers387906506
Maprs387906506
PheGenIrs387906506
hapmaprs387906506
1000 genomesrs387906506
hgdprs387906506
ensemblrs387906506
gopubmedrs387906506
geneviewrs387906506
scholarrs387906506
googlers387906506
pharmgkbrs387906506
gwascentralrs387906506
openSNPrs387906506
23andMers387906506
23andMe allrs387906506
SNP Nexus

SNPshotrs387906506
SNPdbers387906506
MSV3drs387906506
GWAS Ctlgrs387906506
Max Magnitude0
ClinVar
Risk rs387906506(;)
Alt rs387906506(;)
Reference rs387906506(C;C)
Significance Pathogenic
Disease Factor X deficiency
Variation info
Gene F10
CLNDBN Factor X deficiency
Reversed 0
HGVS NC_000013.10:g.113801758delC
CLNSRC OMIM Allelic Variant
CLNACC RCV000012834.4,