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rs137852233

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs137852233(A;A)
Make rs137852233(A;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position139541114
GeneF9
is asnp
is mentioned by
dbSNPrs137852233
ebirs137852233
HLIrs137852233
Exacrs137852233
Varsomers137852233
Maprs137852233
PheGenIrs137852233
hapmaprs137852233
1000 genomesrs137852233
hgdprs137852233
ensemblrs137852233
gopubmedrs137852233
geneviewrs137852233
scholarrs137852233
googlers137852233
pharmgkbrs137852233
gwascentralrs137852233
openSNPrs137852233
23andMers137852233
23andMe allrs137852233
SNP Nexus

SNPshotrs137852233
SNPdbers137852233
MSV3drs137852233
GWAS Ctlgrs137852233
Max Magnitude0
OMIM300746
Desc
Variant0022
Relatedalso
ClinVar
Risk rs137852233(A;A)
Alt rs137852233(A;A)
Reference rs137852233(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.138623273G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000011325.7,