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rs137852226

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs137852226(A;T)
Make rs137852226(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position139537139
GeneF9
is asnp
is mentioned by
dbSNPrs137852226
ebirs137852226
HLIrs137852226
Exacrs137852226
Varsomers137852226
Maprs137852226
PheGenIrs137852226
hapmaprs137852226
1000 genomesrs137852226
hgdprs137852226
ensemblrs137852226
gopubmedrs137852226
geneviewrs137852226
scholarrs137852226
googlers137852226
pharmgkbrs137852226
gwascentralrs137852226
openSNPrs137852226
23andMers137852226
23andMe allrs137852226
SNP Nexus

SNPshotrs137852226
SNPdbers137852226
MSV3drs137852226
GWAS Ctlgrs137852226
Max Magnitude0
OMIM300746
Desc
Variant0014
Relatedalso
ClinVar
Risk rs137852226(T;T)
Alt rs137852226(T;T)
Reference rs137852226(A;A)
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.138619298A>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000011317.7,