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rs137852267

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs137852267(A;A)
Make rs137852267(A;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position139562009
GeneF9
is asnp
is mentioned by
dbSNPrs137852267
ebirs137852267
HLIrs137852267
Exacrs137852267
Varsomers137852267
Maprs137852267
PheGenIrs137852267
hapmaprs137852267
1000 genomesrs137852267
hgdprs137852267
ensemblrs137852267
gopubmedrs137852267
geneviewrs137852267
scholarrs137852267
googlers137852267
pharmgkbrs137852267
gwascentralrs137852267
openSNPrs137852267
23andMers137852267
23andMe allrs137852267
SNP Nexus

SNPshotrs137852267
SNPdbers137852267
MSV3drs137852267
GWAS Ctlgrs137852267
Max Magnitude0
OMIM300746
Desc
Variant0068
Relatedalso
ClinVar
Risk rs137852267(A;A)
Alt rs137852267(A;A)
Reference rs137852267(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.138644168G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000011370.3,