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rs387906476

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs387906476(A;T)
Make rs387906476(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position139530844
GeneF9
is asnp
is mentioned by
dbSNPrs387906476
ebirs387906476
HLIrs387906476
Exacrs387906476
Varsomers387906476
Maprs387906476
PheGenIrs387906476
hapmaprs387906476
1000 genomesrs387906476
hgdprs387906476
ensemblrs387906476
gopubmedrs387906476
geneviewrs387906476
scholarrs387906476
googlers387906476
pharmgkbrs387906476
gwascentralrs387906476
openSNPrs387906476
23andMers387906476
23andMe allrs387906476
SNP Nexus

SNPshotrs387906476
SNPdbers387906476
MSV3drs387906476
GWAS Ctlgrs387906476
Max Magnitude0
ClinVar
Risk rs387906476(T;T)
Alt rs387906476(T;T)
Reference rs387906476(A;A)
Significance Pathogenic
Disease Hereditary factor IX deficiency disease
Variation info
Gene
CLNDBN Hereditary factor IX deficiency disease
Reversed 0
HGVS NC_000023.10:g.138613003A>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000011317.1,