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rs137852255

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs137852255(C;C)
Make rs137852255(C;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position139561743
GeneF9
is asnp
is mentioned by
dbSNPrs137852255
ebirs137852255
HLIrs137852255
Exacrs137852255
Varsomers137852255
Maprs137852255
PheGenIrs137852255
hapmaprs137852255
1000 genomesrs137852255
hgdprs137852255
ensemblrs137852255
gopubmedrs137852255
geneviewrs137852255
scholarrs137852255
googlers137852255
pharmgkbrs137852255
gwascentralrs137852255
openSNPrs137852255
23andMers137852255
23andMe allrs137852255
SNP Nexus

SNPshotrs137852255
SNPdbers137852255
MSV3drs137852255
GWAS Ctlgrs137852255
Max Magnitude0
OMIM300746
Desc
Variant0051
Relatedalso
ClinVar
Risk rs137852255(C;C)
Alt rs137852255(C;C)
Reference rs137852255(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.138643902T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000011354.6,