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rs137852257

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs137852257(A;A)
Make rs137852257(A;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position139561754
GeneF9
is asnp
is mentioned by
dbSNPrs137852257
ebirs137852257
HLIrs137852257
Exacrs137852257
Varsomers137852257
Maprs137852257
PheGenIrs137852257
hapmaprs137852257
1000 genomesrs137852257
hgdprs137852257
ensemblrs137852257
gopubmedrs137852257
geneviewrs137852257
scholarrs137852257
googlers137852257
pharmgkbrs137852257
gwascentralrs137852257
openSNPrs137852257
23andMers137852257
23andMe allrs137852257
SNP Nexus

SNPshotrs137852257
SNPdbers137852257
MSV3drs137852257
GWAS Ctlgrs137852257
Max Magnitude0
OMIM300746
Desc
Variant0054
Relatedalso
ClinVar
Risk rs137852257(A;A)
Alt rs137852257(A;A)
Reference rs137852257(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.138643913G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000011357.7,