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rs387906475

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs387906475(A;A)
Make rs387906475(A;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position139530843
GeneF9
is asnp
is mentioned by
dbSNPrs387906475
ebirs387906475
HLIrs387906475
Exacrs387906475
Varsomers387906475
Maprs387906475
PheGenIrs387906475
hapmaprs387906475
1000 genomesrs387906475
hgdprs387906475
ensemblrs387906475
gopubmedrs387906475
geneviewrs387906475
scholarrs387906475
googlers387906475
pharmgkbrs387906475
gwascentralrs387906475
openSNPrs387906475
23andMers387906475
23andMe allrs387906475
SNP Nexus

SNPshotrs387906475
SNPdbers387906475
MSV3drs387906475
GWAS Ctlgrs387906475
Max Magnitude0
ClinVar
Risk rs387906475(A;A)
Alt rs387906475(A;A)
Reference rs387906475(G;G)
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.138613002G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000011316.7,