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rs587776735

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs587776735(C;C)
Make rs587776735(C;T)
ReferenceGRCh38 38.1/142
ChromosomeX
Position139537388
GeneF9
is asnp
is mentioned by
dbSNPrs587776735
ebirs587776735
HLIrs587776735
Exacrs587776735
Varsomers587776735
Maprs587776735
PheGenIrs587776735
hapmaprs587776735
1000 genomesrs587776735
hgdprs587776735
ensemblrs587776735
gopubmedrs587776735
geneviewrs587776735
scholarrs587776735
googlers587776735
pharmgkbrs587776735
gwascentralrs587776735
openSNPrs587776735
23andMers587776735
23andMe allrs587776735
SNP Nexus

SNPshotrs587776735
SNPdbers587776735
MSV3drs587776735
GWAS Ctlgrs587776735
Max Magnitude0
ClinVar
Risk rs587776735(C;C)
Alt rs587776735(C;C)
Reference rs587776735(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.138619547T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000011409.5,