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rs387906481

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs387906481(C;C)
Make rs387906481(C;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position139530846
GeneF9
is asnp
is mentioned by
dbSNPrs387906481
ebirs387906481
HLIrs387906481
Exacrs387906481
Varsomers387906481
Maprs387906481
PheGenIrs387906481
hapmaprs387906481
1000 genomesrs387906481
hgdprs387906481
ensemblrs387906481
gopubmedrs387906481
geneviewrs387906481
scholarrs387906481
googlers387906481
pharmgkbrs387906481
gwascentralrs387906481
openSNPrs387906481
23andMers387906481
23andMe allrs387906481
SNP Nexus

SNPshotrs387906481
SNPdbers387906481
MSV3drs387906481
GWAS Ctlgrs387906481
Max Magnitude0
ClinVar
Risk rs387906481(C;C)
Alt rs387906481(C;C)
Reference rs387906481(T;T)
Significance Pathogenic
Disease Hereditary factor IX deficiency disease
Variation info
Gene F9
CLNDBN Hereditary factor IX deficiency disease
Reversed 0
HGVS NC_000023.10:g.138613005T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000011402.3,