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rs387906477

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs387906477(G;T)
Make rs387906477(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position139551082
GeneF9
is asnp
is mentioned by
dbSNPrs387906477
ebirs387906477
HLIrs387906477
Exacrs387906477
Varsomers387906477
Maprs387906477
PheGenIrs387906477
hapmaprs387906477
1000 genomesrs387906477
hgdprs387906477
ensemblrs387906477
gopubmedrs387906477
geneviewrs387906477
scholarrs387906477
googlers387906477
pharmgkbrs387906477
gwascentralrs387906477
openSNPrs387906477
23andMers387906477
23andMe allrs387906477
SNP Nexus

SNPshotrs387906477
SNPdbers387906477
MSV3drs387906477
GWAS Ctlgrs387906477
Max Magnitude0
ClinVar
Risk rs387906477(T;T)
Alt rs387906477(T;T)
Reference rs387906477(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.138633241G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000011338.7,