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rs587776736

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AG;AG) 0 common in clinvar
Make rs587776736(-;-)
Make rs587776736(-;AG)
ReferenceGRCh38 38.1/142
ChromosomeX
Position139551081
GeneF9
is asnp
is mentioned by
dbSNPrs587776736
ebirs587776736
HLIrs587776736
Exacrs587776736
Varsomers587776736
Maprs587776736
PheGenIrs587776736
hapmaprs587776736
1000 genomesrs587776736
hgdprs587776736
ensemblrs587776736
gopubmedrs587776736
geneviewrs587776736
scholarrs587776736
googlers587776736
pharmgkbrs587776736
gwascentralrs587776736
openSNPrs587776736
23andMers587776736
23andMe allrs587776736
SNP Nexus

SNPshotrs587776736
SNPdbers587776736
MSV3drs587776736
GWAS Ctlgrs587776736
Max Magnitude0
ClinVar
Risk rs587776736(;)
Alt rs587776736(;)
Reference rs587776736(AG;AG)
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.138633240_138633241delAG
CLNSRC OMIM Allelic Variant
CLNACC RCV000011412.5,