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rs387906478

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs387906478(A;A)
Make rs387906478(A;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position139551238
GeneF9
is asnp
is mentioned by
dbSNPrs387906478
ebirs387906478
HLIrs387906478
Exacrs387906478
Varsomers387906478
Maprs387906478
PheGenIrs387906478
hapmaprs387906478
1000 genomesrs387906478
hgdprs387906478
ensemblrs387906478
gopubmedrs387906478
geneviewrs387906478
scholarrs387906478
googlers387906478
pharmgkbrs387906478
gwascentralrs387906478
openSNPrs387906478
23andMers387906478
23andMe allrs387906478
SNP Nexus

SNPshotrs387906478
SNPdbers387906478
MSV3drs387906478
GWAS Ctlgrs387906478
Max Magnitude0
ClinVar
Risk rs387906478(A;A)
Alt rs387906478(A;A)
Reference rs387906478(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.138633397G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000011347.2,