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rs387906482

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs387906482(C;C)
Make rs387906482(C;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position139561716
GeneF9
is asnp
is mentioned by
dbSNPrs387906482
ebirs387906482
HLIrs387906482
Exacrs387906482
Varsomers387906482
Maprs387906482
PheGenIrs387906482
hapmaprs387906482
1000 genomesrs387906482
hgdprs387906482
ensemblrs387906482
gopubmedrs387906482
geneviewrs387906482
scholarrs387906482
googlers387906482
pharmgkbrs387906482
gwascentralrs387906482
openSNPrs387906482
23andMers387906482
23andMe allrs387906482
SNP Nexus

SNPshotrs387906482
SNPdbers387906482
MSV3drs387906482
GWAS Ctlgrs387906482
Max Magnitude0
ClinVar
Risk rs387906482(C;C)
Alt rs387906482(C;C)
Reference rs387906482(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.138643875T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000011410.6,