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rs137852279

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs137852279(A;T)
Make rs137852279(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position139561557
GeneF9
is asnp
is mentioned by
dbSNPrs137852279
ebirs137852279
HLIrs137852279
Exacrs137852279
Varsomers137852279
Maprs137852279
PheGenIrs137852279
hapmaprs137852279
1000 genomesrs137852279
hgdprs137852279
ensemblrs137852279
gopubmedrs137852279
geneviewrs137852279
scholarrs137852279
googlers137852279
pharmgkbrs137852279
gwascentralrs137852279
openSNPrs137852279
23andMers137852279
23andMe allrs137852279
SNP Nexus

SNPshotrs137852279
SNPdbers137852279
MSV3drs137852279
GWAS Ctlgrs137852279
Max Magnitude0
OMIM300746
Desc
Variant0096
Relatedalso
ClinVar
Risk rs137852279(T;T)
Alt rs137852279(T;T)
Reference rs137852279(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.138643716A>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000011398.5,