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rs104894392

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs104894392(C;T)
Make rs104894392(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position113149146
GeneF10
is asnp
is mentioned by
dbSNPrs104894392
ebirs104894392
HLIrs104894392
Exacrs104894392
Varsomers104894392
Maprs104894392
PheGenIrs104894392
hapmaprs104894392
1000 genomesrs104894392
hgdprs104894392
ensemblrs104894392
gopubmedrs104894392
geneviewrs104894392
scholarrs104894392
googlers104894392
pharmgkbrs104894392
gwascentralrs104894392
openSNPrs104894392
23andMers104894392
23andMe allrs104894392
SNP Nexus

SNPshotrs104894392
SNPdbers104894392
MSV3drs104894392
GWAS Ctlgrs104894392
Max Magnitude0
OMIM227600
Desc
Variant0001
Relatedalso
ClinVar
Risk rs104894392(T;T)
Alt rs104894392(T;T)
Reference rs104894392(C;C)
Significance Pathogenic
Disease Factor X deficiency
Variation info
Gene F10
CLNDBN Factor X deficiency
Reversed 0
HGVS NC_000013.10:g.113803460C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000012833.4,